Projects: pypi: browser
https://packages.ecosyste.ms/registries/pypi.org/packages/browser
A package to prevent Dependency Confusion attacks against Yandex.
2 versions
Latest release: over 3 years ago
2 dependent packages
Enhanced Analysis
Repository Activity:
Repository Owner:
Francis Tseng (user)
(〜 ̄▽ ̄)〜☆゚*・。*・*・。*・
(〜 ̄▽ ̄)〜☆゚*・。*・*・。*・
Science Score: 65/100
Starting Score: 100 points
Penalties:
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-10
PyPI ecosystem
General-purpose ecosystem -
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No science terms in description
No scientific terms found in description
Very Likely Science (65)
Papers Mentioning browser 2,125
10.3389/fcell.2021.700029
LncRNA DGCR5 Isoform-1 Silencing Suppresses the Malignant Phenotype of Clear Cell Renal Cell Carcinoma via miR-211-5p/Snail Signal AxisCited by: 9
Author(s): Guangxin Zhong, Dan Luo, Yijun Fan, Jue Wang, Bingqiang Liu, Zhonghua Xu, Xiang Zhang
Software Mentions: 1
Published: about 5 years ago
10.1186/s13039-014-0075-6
Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probesCited by: 10
Author(s): Carla Sustek D’Angelo, Monica Castro Varela, Cláudia Irene Emílio de Castro, Chong Kim, Débora Romeo Bertola, Charles Marques Lourenço, Ana Beatriz Alvarez Perez, Célia Priszkulnik Koiffmann
Software Mentions: 1
Published: almost 12 years ago
10.3389/fcimb.2019.00175
Diverse Papillomavirus Types Induce Endosomal TubulationCited by: 4
Author(s): Abida Siddiqa, Paola Massimi, David Pim, Lawrence Banks
Software Mentions: 1
Published: over 7 years ago
10.3389/fncel.2015.00142
Inducible and combinatorial gene manipulation in mouse brainCited by: 10
Author(s): Godwin Dogbevia, Ricardo Marticorena-Alvarez, Melanie Bausen, Rolf Sprengel, Mazahir T. Hasan
Software Mentions: 1
Published: over 11 years ago
10.1186/1755-8166-1-11
Chromosomal assignment of canine THADA gene to CFA 10q25Cited by: 3
Author(s): Jan T. Soller, Claudia Beuing, Hugo Murua Escobar, Susanne Winkler, Nicola Reimann-Berg, Norbert Drieschner, G. Dolf, C. Schelling, Ingo Nolte, Jörn Bullerdiek
Software Mentions: 1
Published: over 18 years ago
10.3389/fendo.2021.648844
Vitamin D Level and Vitamin D Receptor Genetic Variation Were Involved in the Risk of Non-Alcoholic Fatty Liver Disease: A Case-Control StudyCited by: 5
Author(s): Ru Zhang, Minxian Wang, Min Wang, Liuxin Zhang, Yajie Ding, Zongzhe Tang, Zuqiang Fu, Haozhi Fan, Wei Zhang, Jie Wang
Software Mentions: 1
Published: about 5 years ago
10.3389/fendo.2019.00213
Analysis of the Role of the Mc4r System in Development, Growth, and Puberty of MedakaCited by: 16
Author(s): Ruiqi Liu, Masato Kinoshita, Mateus Contar Adolfi, Manfred Schartl
Software Mentions: 1
Published: over 7 years ago
10.18632/oncotarget.28037
Diverse transcriptional regulation and functional effects revealed by CRISPR/Cas9-directed epigenetic editingCited by: 3
Author(s): Miguel Vizoso, Jacco van Rheenen
Software Mentions: 1
Published: about 5 years ago
10.3389/fendo.2018.00195
Glial Cells Missing 1 Regulates Equine Chorionic Gonadotrophin Beta Subunit via Binding to the Proximal PromoterCited by: 2
Author(s): Jordan E. Read, Victoria Cabrera-Sharp, Phoebe Kitscha, Judith E. Cartwright, Peter King, Robert C. Fowkes, Amanda M. de Mestre
Software Mentions: 1
Published: over 8 years ago
10.3390/jpm11060468
Association of LINC00673 Genetic Variants with Progression of Oral CancerCited by: 15
Author(s): Shih‐Chi Su, Chiao‐Wen Lin, Po‐Chung Ju, Lun‐Ching Chang, Chun‐Yi Chuang, Yu-Fan Liu, Ming‐Ju Hsieh
Software Mentions: 1
Published: over 5 years ago
10.3389/fgene.2021.707644
Suppression of CPSF6 Enhances Apoptosis Through Alternative Polyadenylation-Mediated Shortening of the VHL 3′UTR in Gastric Cancer CellsCited by: 8
Author(s): Xinglong Shi, Keshuo Ding, Qiang Zhao, Pengxiao Li, Yani Kang, Sheng Tan, Jingyong Sun
Software Mentions: 1
Published: almost 5 years ago
10.1186/s13039-017-0308-6
Incidence of the 22q11.2 deletion in a large cohort of miscarriage samplesCited by: 25
Author(s): Melissa Maisenbacher, Katrina Merrion, B. Pettersen, Michael Young, Kiyoung Paik, Sushma Iyengar, Stephanie Kareht, Styrmir Sigurjonsson, Zachary Demko, Kimberly Martin
Software Mentions: 1
Published: over 9 years ago
10.3390/jpm11030231
The Epidemiology and Genetics of Hyperuricemia and Gout across Major Racial Groups: A Literature Review and Population Genetics Secondary Database AnalysisCited by: 45
Author(s): Faven Butler, Ali Alghubayshi, Youssef M Roman
Software Mentions: 1
Published: over 5 years ago
10.3389/fgene.2013.00054
Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum DisordersCited by: 36
Author(s): Mette Gilling, Hanne B. Rasmussen, Kirstine Calloe, Ana Filipa Sequeira, Marta Baretto, Guiomar Oliveira, Joana Almeida, Marlene Briciet Lauritsen, Reinhard Ullmann, Susanne E. Boonen, Karen Brøndum‐Nielsen, Vera M. Kalscheuer, Zeynep Tümer, Astrid M. Vicente, Nicole Schmitt, Niels Tommerup
Software Mentions: 1
Published: over 13 years ago
10.3389/fgene.2019.01105
Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular AtrophyCited by: 2
Author(s): Mingjue Zhao, Mulias Lian, Foong Koon Cheah, Arnold S.C. Tan, Anupriya Agarwal, Samuel S. Chong
Software Mentions: 1
Published: almost 7 years ago
10.1186/s40101-018-0169-7
Association of EGLN1 genetic polymorphisms with SpO2 responses to acute hypobaric hypoxia in a Japanese cohortCited by: 13
Author(s): Yoshiki Yasukochi, Takayuki Nishimura, Midori Motoi, Shigeki Watanuki
Software Mentions: 1
Published: over 8 years ago
10.1186/s13039-015-0153-4
High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemiaCited by: 16
Author(s): Moneeb A.K. Othman, Joana B. Melo, Isabel M. Carreira, Martina Rinčić, Anita Glaser, Beata Grygalewicz, Bernd Gruhn, Kathleen Wilhelm, Katharina Rittscher, Britta Meyer, Maria Luíza Macedo Silva, Terezinha de Jesus Marques Salles, Thomas Liehr
Software Mentions: 1
Published: about 11 years ago
10.3389/fgene.2019.00547
Novel SCN5A Frameshift Mutation in Brugada Syndrome Associated With Complex Arrhythmic PhenotypeCited by: 9
Author(s): Emanuele Micaglio, Michelle M. Monasky, Giuseppe Ciconte, Gabriele Vicedomini, Manuel Conti, Valerio Mecarocci, Luigi Giannelli, Federica Giordano, Alberto Pollina, Massimo Saviano, Paolo Pozzi, Chiara Di Resta, Sara Benedetti, Maurizio Ferrari, Vincenzo Santinelli, Carlo Pappone
Software Mentions: 1
Published: over 7 years ago
10.1186/s13039-020-00510-5
Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature reviewCited by: 2
Author(s): Emiy Yokoyama, Camilo E. Villarroel, Sinhué Diaz, Victoria del Castillo, Patricia Pérez-Vera, Consuelo Salas-Labadía, S Gómez, Reneé Barreda, Bertha Molina, Sara Frías
Software Mentions: 1
Published: about 6 years ago
10.3389/fgene.2021.699894
Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in Chinese PatientsCited by: 2
Author(s): Ying Peng, Changbiao Liang, Hui Xi, Shunli Yang, Junfeng Hu, Jialun Pang, Jing Liu, Yingchun Luo, Chengyuan Tang, Wanqin Xie, Hua Wang
Software Mentions: 1
Published: about 5 years ago
10.3389/fgene.2020.627007
Human Ubiquitin-Specific Peptidase 18 Is Regulated by microRNAs via the 3'Untranslated Region, A Sequence Duplicated in Long Intergenic Non-coding RNA Genes Residing in chr22q11.21Cited by: 11
Author(s): Erminia Rubino, Melania Cruciani, Nicolas Tchitchek, Anna Le Tortorec, Antoine Rolland, Önay Veli, Leslie Vallet, Giulia Gaggi, Frédérique Michel, Nathalie Dejucq-Rainsford, Sandra Pellegrini
Software Mentions: 1
Published: over 5 years ago
10.3389/fgene.2014.00344
Nuclear and mitochondrial tRNA-lookalikes in the human genomeCited by: 32
Author(s): Aristeidis G. Telonis, Phillipe Loher, Yohei Kirino, Isidore Rigoutsos
Software Mentions: 1
Published: almost 12 years ago
10.3389/fgene.2020.00967
Ethnic and Adipose Depot Specific Associations Between DNA Methylation and Metabolic RiskCited by: 7
Author(s): Carmen Pheiffer, Tarryn Willmer, Stephanie Dias, Yoonus Abrahams, Johan Louw, Julia H. Goedecke
Software Mentions: 1
Published: almost 6 years ago
10.3389/fgene.2018.00009
An Update on Phosphodiesterase Mutations Underlying Genetic Etiology of Hearing Loss and Retinitis PigmentosaCited by: 4
Author(s): Rahul Mittal, Nicole Bencie, James M. Parrish, George Liu, Jeenu Mittal, Denise Yan, Xue Zhong Liu
Software Mentions: 1
Published: over 8 years ago
10.1186/s13039-021-00554-1
Terminal 10q26.12 deletion is associated with neonatal asymmetric crying facies syndrome: a case report and literature reviewCited by: 0
Author(s): Qinghong Li, Chunmei Sun, Jinzhen Guo, Zhang Wen, Liping Zhang
Software Mentions: 1
Published: about 5 years ago
10.1098/rsob.120054
Transcriptome sequencing of black grouse ( <i>Tetrao tetrix</i> ) for immune gene discovery and microsatellite developmentCited by: 26
Author(s): Biao Wang, Robert Ekblom, Todd A. Castoe, Eleanor P. Jones, Radoslav Kozma, Erik Bongcam‐Rudloff, David D. Pollock, Jacob Höglund
Software Mentions: 1
Published: over 14 years ago
10.1186/s13039-017-0311-y
Molecular cytogenetic characterisation of a novel de novo ring chromosome 6 involving a terminal 6p deletion and terminal 6q duplication in the different arms of the same chromosomeCited by: 10
Author(s): Nikolai Paul Pace, Frideriki Maggouta, Melissa Twigden, Isabella Borg
Software Mentions: 1
Published: over 9 years ago
10.1186/s13039-016-0266-4
Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams’ syndrome patients in Saudi ArabiaCited by: 5
Author(s): Ibtessam R Hussein, Afaf Magbooli, Etimad Huwait, Adeel G. Chaudhary, Rima S Bader, Mamdooh Gari, Fai T. Ashgan, Maha Mohsin Al-Quaiti, Adel M. Abuzenadah, Mohammed Al‐Qahtani
Software Mentions: 1
Published: about 10 years ago
10.3390/genes12020141
Characterization of Copy-Number Variations and Possible Candidate Genes in Recurrent Pregnancy LossesCited by: 13
Author(s): Yan‐Ran Sheng, Shunyu Hou, Wenting Hu, Chunyan Wei, Yukai Liu, Yuyin Liu, Lu Jiang, Jingjing Xiang, Xiaoxi Sun, Lei Chen, Huiling Wang, Xiao‐Yong Zhu
Software Mentions: 1
Published: over 5 years ago
10.3390/genes12020238
Evolution of the IRF Family in SalmonidsCited by: 7
Author(s): Thomas C. Clark, Pierre Boudinot, Bertrand Collet
Software Mentions: 1
Published: over 5 years ago
10.3390/genes12030430
Hunting for Familial Parkinson’s Disease Mutations in the Post Genome EraCited by: 2
Author(s): Steven Bentley, Ilaria Guella, Holly E. Sherman, Hannah M. Neuendorf, Alex M. Sykes, Javed Fowdar, Peter A. Silburn, Stephen A. Wood, Matthew J. Farrer, George D. Mellick
Software Mentions: 1
Published: over 5 years ago
10.3390/genes12040470
Emerging Role of ODC1 in Neurodevelopmental Disorders and Brain DevelopmentCited by: 13
Author(s): Jeremy W. Prokop, Caleb Bupp, Austin Frisch, Stephanie M. Bilinovich, Daniel B. Campbell, Daniel Vogt, Chad R. Schultz, Katie Uhl, Elizabeth VanSickle, Surender Rajasekaran, André S. Bachmann
Software Mentions: 1
Published: over 5 years ago
10.3390/genes12050669
Investigating Olfactory Gene Variation and Odour Identification in Older AdultsCited by: 4
Author(s): Siddharth Raj, Anbupalam Thalamuthu, Nicola J. Armstrong, Margaret J. Wright, John B. Kwok, Julian N. Trollor, David Ames, Peter R. Schofield, Henry Brodaty, Perminder S. Sachdev, Karen A. Mather
Software Mentions: 1
Published: over 5 years ago
10.3390/genes12060877
Cytogenetic and Array-CGH Characterization of a Simple Case of Reciprocal t(3;10) Translocation Reveals a Hidden Deletion at 5q12Cited by: 0
Author(s): Angelo Cellamare, Nicoletta Coccaro, Maria Cristina Nuzzi, Paola Casieri, Marilina Tampoia, Flavia Angela Maria Maggiolini, Mattia Gentile, Romina Ficarella, Emanuela Ponzi, Maria Rosa Conserva, Laura Cardarelli, Annunziata Panarese, Francesca Antonacci, Antonia Gesario
Software Mentions: 1
Published: over 5 years ago
10.3390/genes12060805
Generation and Genetic Correction of USH2A c.2299delG Mutation in Patient-Derived Induced Pluripotent Stem CellsCited by: 13
Author(s): Xuezhong Liu, Justin Lillywhite, Wenliang Zhu, Zaohua Huang, Andrew E. Clark, Nicholas C. Gosstola, Colin T. Maguire, Derek M. Dykxhoorn, Zheng-Yi Chen, Jun Yang
Software Mentions: 1
Published: over 5 years ago
10.3390/genes12060822
Novel Structural Variation and Evolutionary Characteristics of Chloroplast tRNA in Gossypium PlantsCited by: 6
Author(s): Tingting Zhang, Yang Yang, Xiaoyu Song, Xinyu Gao, Xianliang Zhang, Junjie Zhao, Kehai Zhou, Chun-Chao Zhao, Wei Li, Daigang Yang, Xiongfeng Ma, Zhong-Hu Li
Software Mentions: 1
Published: over 5 years ago
10.3390/genes12081284
Development and Evaluation of the Ancestry Informative Marker Panel of the VISAGE Basic ToolCited by: 18
Author(s): M. de la Puente, Jorge Ruiz-Ramírez, A. Ambroa-Conde, Catarina Xavier, Jacobo Pardo‐Seco, José Antonio Álvarez‐Dios, Ana Freire-Aradas, Ana Mosquera-Miguel, T.E. Gross, Elaine Y.Y. Cheung, Wojciech Branicki, Michael Nothnagel, Walther Parson, Peter M. Schneider, Manfred Kayser, Ángel Carracedo, Marı́a Victoria Lareu, Christopher Phillips
Software Mentions: 1
Published: about 5 years ago
10.3390/genes12081111
Molecular Characterization of Choroideremia-Associated Deletions Reveals an Unexpected Regulation of CHM Gene TranscriptionCited by: 2
Author(s): Tiziana Fioretti, Valentina Di Iorio, Barbara Lombardo, Francesca De Falco, Armando Cevenini, Fabio Cattaneo, Francesco Testa, Lucio Pastore, Francesca Simonelli, Gabriella Esposito
Software Mentions: 1
Published: about 5 years ago
10.3390/genes12081140
Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin TribeCited by: 1
Author(s): Orna Staretz‐Chacham, Shirly Amar, Shlomo Almashanu, Ben Pode‐Shakked, Ann Saada, Ohad Wormser, Eli Hershkovitz
Software Mentions: 1
Published: about 5 years ago
10.1074/mcp.RA117.000155
Detection of Proteome Diversity Resulted from Alternative Splicing is Limited by Trypsin Cleavage SpecificityCited by: 68
Author(s): Xiaojing Wang, Simona G. Codreanu, Bo Wen, Kai Li, Matthew Chambers, D.C. Liebler, Bing Zhang
Software Mentions: 1
Published: over 8 years ago
10.1002/gcc.21943
The miR‐17‐92 cluster and its target <i>THBS1</i> are differentially expressed in angiosarcomas dependent on <i>MYC</i> amplificationCited by: 93
Author(s): Antoîne Italiano, Rachael Thomas, Matthew Breen, Lei Zhang, Aimeé M. Crago, Samuel Singer, Raya Khanin, Robert G. Maki, Aleksandra Mihailović, Markus Hafner, Tom Tuschl, Cristina R. Antonescu
Software Mentions: 1
Published: over 14 years ago
10.1002/dvg.22008
From expression cloning to gene modeling: The development of<i>Xenopus</i>gene sequence resourcesCited by: 19
Author(s): Michael J. Gilchrist
Software Mentions: 1
Published: over 14 years ago
10.1590/1678-4685-GMB-2018-0173
Integrated analysis of the critical region 5p15.3–p15.2 associated with cri-du-chat syndromeCited by: 13
Author(s): Thiago Corrêa, Bruno César Feltes, Mariluce Riegel
Software Mentions: 1
Published: over 7 years ago
10.4061/2011/976398
Application of Microarray-Based Comparative Genomic Hybridization in Prenatal and Postnatal Settings: Three Case ReportsCited by: 5
Author(s): Jing Liu, François Bernier, Julie Lauzon, R. Brian Lowry, Judy Chernos
Software Mentions: 1
Published: about 15 years ago
10.1186/gb-2006-7-s1-s12
Cited by: 507Author(s): Danielle Thierry-Mieg, Jean Thierry‐Mieg
Software Mentions: 1
Published: over 20 years ago
10.1186/gb-2007-8-3-r41
A haplome alignment and reference sequence of the highly polymorphic Ciona savignyi genomeCited by: 97
Author(s): Kerrin S. Small, Michael Brudno, M. Manuela Hill, Arend Sidow
Software Mentions: 1
Published: over 19 years ago
10.1186/gb-2007-8-7-r129
FlyMine: an integrated database for Drosophila and Anopheles genomicsCited by: 345
Author(s): Rachel Lyne, Richard J. Smith, Kim Rutherford, Matthew Wakeling, Andrew Varley, Francois Guillier, Hilde Janssens, Wenyan Ji, P.G. McLaren, Philip North, Rana Debashis, T. V. Riley, Julie Sullivan, Xavier Watkins, Mark Woodbridge, Kathryn S. Lilley, Steven Russell, Michael Ashburner, Kenji Mizuguchi, Gos Micklem
Software Mentions: 1
Published: over 19 years ago
10.1186/gb-2007-8-7-r152
Using comparative genomics to reorder the human genome sequence into a virtual sheep genomeCited by: 84
Author(s): Brian P. Dalrymple, Ewen F. Kirkness, Mikhail Nefedov, Sean McWilliam, Abhirami Ratnakumar, Wes Barris, Shaying Zhao, Jyoti Shetty, J F Maddox, Margaret O'Grady, F. W. Nicholas, A. M. Crawford, Ted Smith, Pieter J. de Jong, John C. McEwan, V. H. Oddy, Noelle E. Cockett
Software Mentions: 1
Published: over 19 years ago
10.1186/gb-2008-9-2-r34
Ancora: a web resource for exploring highly conserved noncoding elements and their association with developmental regulatory genesCited by: 88
Author(s): Pär G. Engström, David Fredman, Boris Lenhard
Software Mentions: 1
Published: over 18 years ago
10.1186/gb-2008-9-2-r37
Sequence context affects the rate of short insertions and deletions in flies and primatesCited by: 47
Author(s): Amos Tanay, Eric D. Siggia
Software Mentions: 1
Published: over 18 years ago
10.1186/gb-2007-8-8-r167
Genomic mapping of Suppressor of Hairy-wing binding sites in DrosophilaCited by: 58
Author(s): Boris Adryan, Gertrud Woerfel, Ian Birch-Machin, Shan Gao, Marie Quick, Lisa Meadows, Steven Russell, Robert A. White
Software Mentions: 1
Published: over 19 years ago
10.1186/gb-2008-9-6-r104
Assignment of isochores for all completely sequenced vertebrate genomes using a consensusCited by: 15
Author(s): Thorsten Schmidt, Dmitrij Frishman
Software Mentions: 1
Published: over 18 years ago
10.1186/gb-2009-10-2-r14
EpiGRAPH: user-friendly software for statistical analysis and prediction of (epi)genomic dataCited by: 51
Author(s): Christoph Bock, Konstantin Halachev, Joachim Büch, Thomas Lengauer
Software Mentions: 1
Published: over 17 years ago
10.1186/gb-2009-10-8-r86
Synorth: exploring the evolution of synteny and long-range regulatory interactions in vertebrate genomesCited by: 25
Author(s): Xianjun Dong, David Fredman, Boris Lenhard
Software Mentions: 1
Published: over 17 years ago
10.1186/gb-2010-11-7-r70
Contrasting chromatin organization of CpG islands and exons in the human genomeCited by: 101
Author(s): Jung Kyoon Choi
Software Mentions: 1
Published: over 16 years ago
10.1186/gb-2011-12-9-r86
Mutation discovery in mice by whole exome sequencingCited by: 102
Author(s): Heather Fairfield, Griffith J Gilbert, Mary Barter, Rebecca R. Corrigan, Michelle Curtain, Yueming Ding, Mark D’Ascenzo, Daniel J. Gerhardt, Chao He, Wenhui Huang, Todd Richmond, Lucy B. Rowe, Frank J. Probst, David E. Bergstrom, Stephen A. Murray, Carol J. Bult, Joel E. Richardson, Benjamin T. Kile, Ivo Gut, Jörg Hager, Snaevar Sigurðsson, Evan Mauceli, Federica Di Palma, Kerstin Lindblad‐Toh, Michael L. Cunningham, Timothy C. Cox, Monica J. Justice, Mona S. Spector, Scott W. Lowe, Thomas Albert, Leah Rae Donahue, Jeffrey A. Jeddeloh, Jay Shendure
Software Mentions: 1
Published: over 15 years ago
10.1186/gb-2011-12-s1-p3
COSMIC: the catalogue of somatic mutations in cancerCited by: 5
Author(s): Nidhi Bindal, Simon Forbes, David Beare, Prasad Gunasekaran, Kenric Leung, Chai Yin Kok, Mingming Jia, Sally Bamford, Charlotte G. Cole, Sari Ward, Jon W. Teague, Michael R. Stratton, Peter J. Campbell, Andrew Futreal
Software Mentions: 1
Published: over 15 years ago
10.1186/gb-2011-12-s1-p24
Identification of functional genetic variants associated with prostate cancer through analysis of genome-wide genetic and epigenetic datasetsCited by: 0
Author(s): McAnthony Tarway, Wei Tang, Ludmila Prokunina–Olsson
Software Mentions: 1
Published: over 15 years ago
10.1186/gb-2012-13-7-r66
Genome and low-iron response of an oceanic diatom adapted to chronic iron limitationCited by: 201
Author(s): Markus Lommer, Michael Specht, Alexandra-Sophie Roy, Lars Kraemer, Reidar Andreson, Magdalena A. Gutowska, Juliane Wolf, Sonja Verena Bergner, Markus B. Schilhabel, Ulrich C. Klostermeier, Robert G. Beiko, Philip Rosenstiel, Michael Hippler, Julie LaRoche
Software Mentions: 1
Published: over 14 years ago
10.1186/gb-2012-13-10-r84
Tissue of origin determines cancer-associated CpG island promoter hypermethylation patternsCited by: 141
Author(s): Duncan Sproul, Robert Kitchen, Colm E. Nestor, JM Dixon, Andrew H. Sims, David J. Harrison, Bernard Ramsahoye, Richard R. Meehan
Software Mentions: 1
Published: over 14 years ago
10.1098/rsob.180131
DNA methylation subpatterns at distinct regulatory regions in human early embryosCited by: 15
Author(s): Rongsong Luo, Chunling Bai, Lei Yang, Zhong Zheng, Guanghua Su, Guang Gao, Zhuying Wei, Yongchun Zuo, Guangpeng Li
Software Mentions: 1
Published: almost 8 years ago
10.1186/gb-2013-14-5-r45
Insights into snoRNA biogenesis and processing from PAR-CLIP of snoRNA core proteins and small RNA sequencingCited by: 115
Author(s): Shivendra Kishore, Andreas Gruber, Dominik J. Jedlinski, Afzal Pasha Syed, Hadi Jorjani, Mihaela Zavolan
Software Mentions: 1
Published: over 13 years ago
10.1186/gb-2013-14-3-r25
Redistribution of H3K27me3 upon DNA hypomethylation results in de-repression of Polycomb target genesCited by: 199
Author(s): James P. Reddington, Sara Maria Perricone, Colm E. Nestor, Judith Reichmann, Neil A. Youngson, Masako Suzuki, Diana Reinhardt, Donncha S. Dunican, James Prendergast, Heidi K. Mjoseng, Bernard Ramsahoye, Emma Whitelaw, John M. Greally, Ian R. Adams, Wendy A. Bickmore, Richard R. Meehan
Software Mentions: 1
Published: over 13 years ago
10.1186/gb-2014-15-1-r5
Mammalian conserved ADAR targets comprise only a small fragment of the human editosomeCited by: 146
Author(s): Yishay Pinto, Haim Y. Cohen, Erez Y. Levanon
Software Mentions: 1
Published: over 12 years ago
10.2174/1874192401711010084
Interpreting the Mechanism of APOE (p.Leu167del) Mutation in the Incidence of Familial Hypercholesterolemia; An In-silico ApproachCited by: 11
Author(s): Omran M. Rashidi, Fatima Amanullah H.Nazar, Mohamed Nabil Alama, Zuhier Awan
Software Mentions: 1
Published: almost 9 years ago
10.1186/gb-2013-14-7-r79
PARma: identification of microRNA target sites in AGO-PAR-CLIP dataCited by: 52
Author(s): Florian Erhard, Lars Dölken, Łukasz Jaśkiewicz, Ralf Zimmer
Software Mentions: 1
Published: over 13 years ago
10.1186/s40348-020-00102-8
Nup133 and ERα mediate the differential effects of hyperoxia-induced damage in male and female OPCsCited by: 7
Author(s): Donna Elizabeth Sunny, Elke Hammer, Sebastian Strempel, Christy Joseph, Himanshu Manchanda, Till Ittermann, Stephanie Hübner, Frank Ulrich Weiß, Uwe Völker, Matthias Heckmann
Software Mentions: 1
Published: about 6 years ago
10.1186/s13059-015-0672-7
Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expressionCited by: 130
Author(s): Ruslan Strogantsev, Felix Krueger, Kazuki Yamazawa, Hui Shi, Poppy A. Gould, Megan Goldman-Roberts, Kirsten McEwen, Bowen Sun, Roger A. Pedersen, Anne C. Ferguson-Smith
Software Mentions: 1
Published: over 11 years ago
10.1186/1750-1172-7-S2-A11
Speeding up research with the Semantic WebCited by: 1
Author(s): Marco Roos, Erik Schultes, Barend Mons
Software Mentions: 1
Published: over 14 years ago
10.1007/s11010-021-04103-7
Evidence of synergism among three genetic variants in a patient with LMNA-related lipodystrophy and amyotrophic lateral sclerosis leading to a remarkable nuclear phenotypeCited by: 3
Author(s): Kathryn Volkening, Sali M.K. Farhan, Jennifer L. Kao, Cheryl Leystra-Lantz, Lee Cyn Ang, Adam D. McIntyre, Jian Wang, Robert A. Hegele, Michael J. Strong
Software Mentions: 1
Published: over 5 years ago
10.1186/s13059-015-0768-0
Chromatin interaction analysis reveals changes in small chromosome and telomere clustering between epithelial and breast cancer cellsCited by: 175
Author(s): A. Rasim Barutcu, Bryan R. Lajoie, Rachel Patton McCord, Coralee E. Tye, Deli Hong, Terri L. Messier, Gillian Browne, André J. van Wijnen, Jane B. Lian, Janet L. Stein, Job Dekker, Anthony N. Imbalzano
Software Mentions: 1
Published: almost 11 years ago
10.1186/s13059-015-0842-7
High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fractionCited by: 106
Author(s): Joseph L. McClay, Andrey A. Shabalin, Mikhail G. Dozmorov, Daniel E. Adkins, Gaurav Kumar, Srilaxmi Nerella, Shaunna L. Clark, Sarah E. Bergen, Christina M. Hultman, Patrik K. E. Magnusson, Patrick F. Sullivan, Karolina A. Åberg, Edwin J. C. G. van den Oord
Software Mentions: 1
Published: almost 11 years ago
10.1186/s13059-016-0876-5
The contribution of Alu exons to the human proteomeCited by: 36
Author(s): Lan Lin, Peng Jiang, Juw Won Park, Jinkai Wang, Zhi-xiang Lu, Maggie P. Y. Lam, Peipei Ping, Yi Xing
Software Mentions: 1
Published: over 10 years ago
10.1186/s13023-015-0251-8
Rare diseases in ICD11: making rare diseases visible in health information systems through appropriate codingCited by: 84
Author(s): Ségolène Aymé, Bertrand Bellet, Ana Rath
Software Mentions: 1
Published: over 11 years ago
10.1186/s13059-017-1185-3
Diverse interventions that extend mouse lifespan suppress shared age-associated epigenetic changes at critical gene regulatory regionsCited by: 141
Author(s): John Cole, Neil Robertson, Mohammed Iqbal Rather, John P. Thomson, Tony McBryan, Duncan Sproul, Tina Wang, Claire Brock, William Clark, Trey Ideker, Richard R. Meehan, Richard A. Miller, Holly M. Brown–Borg, Peter D. Adams
Software Mentions: 1
Published: over 9 years ago
10.1186/s13059-017-1226-y
The developmental regulator PKL is required to maintain correct DNA methylation patterns at RNA-directed DNA methylation lociCited by: 30
Author(s): Rong Yang, Zhimin Zheng, Qing Chen, Lan Yang, Huan Huang, Daisuke Miki, Wenwu Wu, Liang Zeng, Jun Li, Jin‐Xing Zhou, Joe Ogas, Jian‐Kang Zhu, Xin‐Jian He, Heng Zhang
Software Mentions: 1
Published: over 9 years ago
10.1186/s13059-017-1225-z
Regulatory landscape fusion in rhabdomyosarcoma through interactions between the PAX3 promoter and FOXO1 regulatory elementsCited by: 21
Author(s): Cristina Vicente-García, Bárbara Villarejo-Balcells, Ibai Irastorza-Azcárate, Silvia Naranjo, Rafael D. Acemel, Juan J. Tena, Peter Rigby, Damien P. Devos, José Luis Gómez-Skármeta, Jaime J. Carvajal
Software Mentions: 1
Published: about 9 years ago
10.1186/gb-2004-6-1-r9
Cited by: 253Author(s): Frank Desiere, Eric W. Deutsch, Alexey I. Nesvizhskii, Parag Mallick, Nichole L. King, Jimmy K. Eng, Alan Aderem, Rose Boyle, Erich Brunner, Samuel Donohoe, Nelson Fausto, Ernst Hafen, Lee Hood, Michael G. Katze, Kathleen A. Kennedy, Floyd Kregenow, Hookeun Lee, Biaoyang Lin, Dan Martin, Jeffrey A. Ranish, David J. Rawlings, Lawrence E. Samelson, Yuzuru Shiio, Julian D. Watts, Bernd Wollscheid, M. Wright, Wei Yan, Lizhu Yang, Eugene C. Yi, Hui Zhang, Ruedi Aebersold
Software Mentions: 1
Published: over 22 years ago
10.1186/s13059-018-1393-5
The peopling of the last Green Sahara revealed by high-coverage resequencing of trans-Saharan patrilineagesCited by: 30
Author(s): Eugenia D’Atanasio, Beniamino Trombetta, Maria Di Bonito, Andrea Finocchio, Genny Di Vito, Mara Seghizzi, Rita Romano, Gianluca Russo, Giacomo Maria Paganotti, Elizabeth E. Watson, Alfredo Coppa, Paolo Anagnostou, Jean‐Michel Dugoujon, Pedro Moral, Daniele Sellitto, Andrea Novelletto, Fulvio Cruciani
Software Mentions: 1
Published: over 8 years ago
10.1186/s13059-018-1434-0
Negative selection in tumor genome evolution acts on essential cellular functions and the immunopeptidomeCited by: 73
Author(s): Luís Zapata, Oriol Pich, Luís Serrano, Fyodor A. Kondrashov, Stephan Ossowski, Martin H. Schaefer
Software Mentions: 1
Published: over 8 years ago
10.1186/s13059-018-1493-2
Cell type-specific CLIP reveals that NOVA regulates cytoskeleton interactions in motoneuronsCited by: 16
Author(s): Yuan Yuan, Shirley Xie, Jennifer C. Darnell, Andrew J. Darnell, Yuhki Saito, Hemali Phatnani, Elisabeth A. Murphy, Chaolin Zhang, Tom Maniatis, Robert B. Darnell
Software Mentions: 1
Published: about 8 years ago
10.1186/s13059-018-1491-4
Linking the International Wheat Genome Sequencing Consortium bread wheat reference genome sequence to wheat genetic and phenomic dataCited by: 181
Author(s): Michaël Alaux, Jane Rogers, Thomas Letellier, Raphaël Flores, Françoise Alfama, Cyril Pommier, Nacer Mohellibi, Sophie Durand, Erik Kimmel, Célia Michotey, Claire Guerche, Mikaël Loaec, Mathilde Lainé, Delphine Steinbach, Frédéric Choulet, Hélène Rimbert, Philippe Leroy, Nicolas Guilhot, Jérôme Salse, Catherine Feuillet, Etienne Paux, Kellye Eversole, Anne-Françoise Adam-Blondon, Hadi Quesneville
Software Mentions: 1
Published: about 8 years ago
10.1186/s13059-018-1544-8
Reconstruction of avian ancestral karyotypes reveals differences in the evolutionary history of macro- and microchromosomesCited by: 40
Author(s): Joana Damas, Jaebum Kim, Marta Farré, Darren K. Griffin, Denis M. Larkin
Software Mentions: 1
Published: almost 8 years ago
10.1016/j.molcel.2015.01.011
BRCA1 Recruitment to Transcriptional Pause Sites Is Required for R-Loop-Driven DNA Damage RepairCited by: 342
Author(s): Elodie Hatchi, Konstantina Skourti-Stathaki, Steffen Ventz, Luca Pinello, Angela Yen, Kinga Kamieniarz-Gdula, Stoil D. Dimitrov, Shailja Pathania, Kristine McKinney, Matthew L. Eaton, M Kellis, Sarah J. Hill, Giovanni Parmigiani, Nick J. Proudfoot, David M. Livingston
Software Mentions: 1
Published: over 11 years ago
10.1186/s13059-019-1889-7
Chromosome-level genome assembly for giant panda provides novel insights into Carnivora chromosome evolutionCited by: 28
Author(s): Huizhong Fan, Qi Wu, Fuwen Wei, Fengtang Yang, Bee Ling Ng, Yibo Hu
Software Mentions: 1
Published: almost 7 years ago
10.1186/s13059-019-1897-7
PASTMUS: mapping functional elements at single amino acid resolution in human cellsCited by: 6
Author(s): Xinyi Zhang, Di Yue, Yinan Wang, Yan Zhou, Ying Liu, Yu Qiu, Feng Tian, Ying Yu, Zhuo Zhou, Wensheng Wei
Software Mentions: 1
Published: almost 7 years ago
10.1186/1476-4598-13-120
A novel approach to identify driver genes involved in androgen-independent prostate cancerCited by: 44
Author(s): Ellyn N. Schinke, Victor M. Bii, Arun Kumar Nalla, Dustin T. Rae, Laura Tedrick, Gary G. Meadows, Grant D. Trobridge
Software Mentions: 1
Published: over 12 years ago
10.1186/s13059-020-02017-z
ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing dataCited by: 91
Author(s): Egor Dolzhenko, Mark F Bennett, Phillip A. Richmond, Brett Trost, Sai Chen, Joke J.F.A. van Vugt, Charlotte Nguyen, Giuseppe Narzisi, Vladimir G. Gainullin, Andrew M. Gross, Bryan R. Lajoie, Ryan J. Taft, Wyeth W. Wasserman, Stephen W. Scherer, Jan H. Veldink, David Bentley, Ryan K. C. Yuen, Melanie Bahlo, Michael A. Eberle
Software Mentions: 1
Published: over 6 years ago
10.1186/s13059-020-02184-z
Deep sequencing reveals a DAP1 regulatory haplotype that potentiates autoimmunity in systemic lupus erythematosusCited by: 7
Author(s): Prithvi Raj, Ran Song, Honglin Zhu, Linley Riediger, Dong Jae Jun, Chao Liang, Carlos Arana, Bo Zhang, Yajing Gao, Benjamin Wakeland, Igor Dozmorov, Jianuan Zhou, Jennifer A. Kelly, Bernard Lauwerys, Joel M. Guthridge, Nancy J. Olsen, Swapan K. Nath, Chandrashekhar Pasare, Nicolai S. C. van Oers, Gary S. Gilkeson, Betty P. Tsao, Patrick M. Gaffney, Peter K. Gregersen, Judith A. James, Xiaoxia Zuo, David R. Karp, Quan Zhen Li, Edward K. Wakeland
Software Mentions: 1
Published: almost 6 years ago
10.1186/s12943-020-01277-4
The PVT1 lncRNA is a novel epigenetic enhancer of MYC, and a promising risk-stratification biomarker in colorectal cancerCited by: 51
Author(s): Kunitoshi Shigeyasu, Shusuke Toden, Tomohiro Ozawa, Takatoshi Matsuyama, Takeshi Nagasaka, Toshiaki Ishikawa, Debashis Sahoo, Pradipta Ghosh, Hiroyuki Uetake, Toshiyoshi Fujiwara, Ajay Goel
Software Mentions: 1
Published: almost 6 years ago
10.1186/1756-6606-4-14
Identification of a novel intronic enhancer responsible for the transcriptional regulation of musashi1 in neural stem/progenitor cellsCited by: 23
Author(s): S. Kawase, Toshio Imai, Chikako Miyauchi-Hara, Kunio Yaguchi, Yoshinori Nishimoto, Shin Ichi Fukami, Yuji Matsuzaki, Atsushi Miyawaki, Shigeyoshi Itohara, Hideyuki Okano
Software Mentions: 1
Published: over 15 years ago
10.1093/gbe/evu139
The Draft Assembly of the Radically Organized Stylonychia lemnae Macronuclear GenomeCited by: 54
Author(s): Samuel H. Aeschlimann, Franziska Jönsson, Jan Postberg, Nicholas A. Stover, Robert L. Petera, Hans-Joachim Lipps, Mariusz Nowacki, Estienne C. Swart
Software Mentions: 1
Published: about 12 years ago
10.1093/gbe/evv012
The Role of DNA Insertions in Phenotypic Differentiation between Humans and Other PrimatesCited by: 4
Author(s): Elizabeth Hellen, Andrew D. Kern
Software Mentions: 1
Published: over 11 years ago
10.1093/gbe/evv142
A Genome-Wide Landscape of Retrocopies in Primate GenomesCited by: 44
Author(s): Fábio C. P. Navarro, Pedro A. F. Galante
Software Mentions: 1
Published: about 11 years ago
10.1093/gbe/evv161
Comparative Genomics of Environmental and Clinical<i>Stenotrophomonas maltophilia</i>Strains with Different Antibiotic Resistance ProfilesCited by: 72
Author(s): Benjamin Youenou, Sabine Favre-Bonté, Josselin Bodilis, Elisabeth Brothier, Audrey Dubost, Daniel Müller, Sylvie Nazaret
Software Mentions: 1
Published: about 11 years ago
10.1093/gbe/evx237
The Diversity of REcent and Ancient huMan (DREAM): A New Microarray for Genetic Anthropology and Genealogy, Forensics, and Personalized MedicineCited by: 9
Author(s): Eran Elhaik, Leeban Yusuf, Ainan I J Anderson, Mehdi Pirooznia, Dimitrios Arnellos, Gregory Vilshansky, Gunes Ercal, Yontao Lu, Teresa A. Webster, Michael L. Baird, Umberto Esposito
Software Mentions: 1
Published: almost 9 years ago
10.1093/gbe/evy199
Turning Vice into Virtue: Using Batch-Effects to Detect Errors in Large Genomic Data SetsCited by: 7
Author(s): Fabrizio Mafessoni, Rashmi B. Prasad, Leif Groop, Ola Hansson, Kay Prüfer
Software Mentions: 1
Published: almost 8 years ago
10.1093/gbe/evz228
A Nearly Complete Genome of Ciona intestinalis Type A (C. robusta) Reveals the Contribution of Inversion to Chromosomal Evolution in the Genus CionaCited by: 69
Author(s): Yutaka Satou, Ryohei Nakamura, Dejie Yu, Reiko Yoshida, Mayuko Hamada, Manabu Fujie, Kanako Hisata, Hiroyuki Takeda, Noriyuki Satoh
Software Mentions: 1
Published: almost 7 years ago
10.1093/gbe/evz254
Genome Assembly of the Dogface Butterfly Zerene cesoniaCited by: 7
Author(s): Luis Rodriguez-Caro, Jennifer Fenner, Caleb Benson, Steven M. Van Belleghem, Brian A. Counterman
Software Mentions: 1
Published: almost 7 years ago
10.1093/gbe/evaa045
Weak Correlation between Nucleotide Variation and Recombination Rate across the House Mouse GenomeCited by: 9
Author(s): Michael Emmett Kartje, Peicheng Jing, Bret A. Payseur
Software Mentions: 1
Published: over 6 years ago