Ecosyste.ms: Papers
An open API service providing mapping between scientific papers and software projects that are mentioned in them.
All mentions data is based on the CZI Software Mentions dataset.
Projects: pypi: bcbio-nextgen
https://packages.ecosyste.ms/registries/pypi.org/packages/bcbio-nextgen
Best-practice pipelines for fully automated high throughput sequencing analysis
57 versions
Latest release: over 5 years ago
160 downloads last month
Papers Mentioning bcbio-nextgen 43
10.1186/s12859-016-1241-0
systemPipeR: NGS workflow and report generation environmentCited by: 148
Author(s): Tyler W. H. Backman, Thomas Girke
Software Mentions: 19
Published: about 8 years ago
10.1186/s12859-017-1770-1
CIPHER: a flexible and extensive workflow platform for integrative next-generation sequencing data analysis and genomic regulatory element predictionCited by: 24
Author(s): Carlos Guzmán, Iván D’Orso
Software Mentions: 10
Published: over 7 years ago
10.1186/s12859-018-2287-y
miRge 2.0 for comprehensive analysis of microRNA sequencing dataCited by: 54
Author(s): Yin Lu, Alexander S. Baras, Marc K. Halushka
Software Mentions: 9
Published: over 6 years ago
10.1038/s41597-019-0095-5
Multi omics analysis of fibrotic kidneys in two mouse modelsCited by: 25
Author(s): Mira Pavkovic, Lorena Pantano, Cory V. Gerlach, Sergine Brutus, Sarah A. Boswell, Robert A. Everley, Jagesh V. Shah, Shannan Ho Sui, Vishal S. Vaidya
Software Mentions: 7
Published: over 5 years ago
10.1371/journal.pone.0072614
DistMap: A Toolkit for Distributed Short Read Mapping on a Hadoop ClusterCited by: 46
Author(s): Ram Vinay Pandey, Christian Schlötterer
Software Mentions: 6
Published: about 11 years ago
10.1016/j.xpro.2020.100079
Using Chromatin Accessibility to Delineate Therapeutic Subtypes in Pancreatic Cancer Patient-Derived Cell LinesCited by: 4
Author(s): Holly Brunton, Ian Garner, Ulla-Maja Bailey, Rosanna Upstill-Goddard, Peter J. Bailey
Software Mentions: 6
Published: about 4 years ago
10.1371/journal.pone.0243807
Optimised generation of iPSC-derived macrophages and dendritic cells that are functionally and transcriptionally similar to their primary counterpartsCited by: 17
Author(s): Susan J. Monkley, Jayendra Kumar Krishnaswamy, Melker Göransson, Maryam Clausen, Johan Meuller, Kristofer Thörn, Ryan Hicks, Stephen Delaney, Louise Stjernborg
Software Mentions: 6
Published: almost 4 years ago
10.1038/s41598-019-40786-1
Integrated analysis of relapsed B-cell precursor Acute Lymphoblastic Leukemia identifies subtype-specific cytokine and metabolic signaturesCited by: 18
Author(s): M. Schroêder, Lorenz Bastian, Cornelia Eckert, Nicola Gökbuget, Alva Rani James, Jutta Ortiz Tanchez, Cornelia Schlee, Konstandina Isaakidis, Björn Häupl, Katharina Baum, Oscar Arturo Migueles Lozano, Khouloud Kouidri, Kuan‐Ting Pan, Henning Urlaub, Stefan Schwartz, Thomas Burmeister, Arend von Stackelberg, Dieter Hoelzer, Heike Pfeiffer, Michael A. Rieger, Stefanie Göllner, Thomas Oellerich, Martin Horstman, Martin Schrappe, Jana Wolf, Renate Kirschner-Schwabe, Monika Brüggemann, Carsten Müller‐Tidow, Hubert Serve, Martin Neumann, Claudia D. Baldus
Software Mentions: 5
Published: over 5 years ago
10.1186/s13059-014-0577-x
Churchill: an ultra-fast, deterministic, highly scalable and balanced parallelization strategy for the discovery of human genetic variation in clinical and population-scale genomicsCited by: 109
Author(s): Benjamin J. Kelly, James Fitch, Yangqiu Patrick Hu, Donald J. Corsmeier, Huachun Zhong, Amy Wetzel, Russell D Nordquist, David L. Newsom, Peter White
Software Mentions: 5
Published: almost 10 years ago
10.1186/s13041-021-00835-1
Altered hippocampal transcriptome dynamics following sleep deprivationCited by: 14
Author(s): Marie E. Gaine, Ethan Bahl, Snehajyoti Chatterjee, Jacob J. Michaelson, Ted Abel, Lisa C. Lyons
Software Mentions: 5
Published: over 3 years ago
10.1530/ERC-19-0474
A xenograft and cell line model of SDH-deficient pheochromocytoma derived from Sdhb+/− ratsCited by: 15
Author(s): James F. Powers, Brent Cochran, James D. Baleja, Hadley D. Sikes, Andrew Pattison, Xue Zhang, Inna Lomakin, Annette Shepard-Barry, Karel Pacák, Sun Jin Moon, Troy F. Langford, Kassi T. Stein, Richard W. Tothill, Ying-Bin Ouyang, Arthur S. Tischler
Software Mentions: 5
Published: over 4 years ago
10.1186/s12859-019-3219-1
uap: reproducible and robust HTS data analysisCited by: 12
Author(s): Christoph Kämpf, Michael Specht, Alexander Scholz, Sven-Holger Puppel, Gero Doose, Kristin Reiche, Jana Schor, Jörg Hackermüller
Software Mentions: 5
Published: almost 5 years ago
10.3389/fnmol.2019.00236
Sex-Dependent Changes in miRNA Expression in the Bed Nucleus of the Stria Terminalis Following StressCited by: 16
Author(s): Maria Mavrikaki, Lorena Pantano, David N. Potter, Maximilian Rogers-Grazado, Eleni Anastasiadou, Frank J. Slack, Sami S. Amr, Kerry J. Ressler, Nikolaos P. Daskalakis, Elena H. Chartoff
Software Mentions: 5
Published: about 5 years ago
10.1186/s12864-020-07218-1
Targeted mutagenesis of ∆5 and ∆6 fatty acyl desaturases induce dysregulation of lipid metabolism in Atlantic salmon (Salmo salar)Cited by: 6
Author(s): Yang Jin, Alex K. Datsomor, Rolf Erik Olsen, Jon Olav Vik, Jacob Torgersen, Rolf B. Edvardsen, Anna Wargelius, Per Winge, Fabian Grammes
Software Mentions: 4
Published: about 4 years ago
10.1186/s12859-015-0795-6
TOGGLE: toolbox for generic NGS analysesCited by: 20
Author(s): Cécile Monat, Christine Tranchant‐Dubreuil, Ayité Kougbeadjo, Cédric Farcy, Enrique Ortega-Abboud, Souhila Amanzougarene, Sébastien Ravel, Mawussé Agbessi, Julie Orjuela, Marilyne Summo, François Sabot
Software Mentions: 4
Published: about 9 years ago
10.1038/s41598-018-25022-6
DNAp: A Pipeline for DNA-seq Data AnalysisCited by: 13
Author(s): Jason Causey, Cody Ashby, Karl Walker, Zhiping Paul Wang, Mary Qu Yang, Yuanfang Guan, Jason H. Moore, Xiuzhen Huang
Software Mentions: 4
Published: over 6 years ago
10.18632/oncotarget.26322
Differential gene expression in human tissue resident regulatory T cells from lung, colon, and bloodCited by: 13
Author(s): Magdalena Niedzielska, Elisabeth Israelsson, B. Angermann, Ben S. Sidders, Maryam Clausen, Matthew C. Catley, Rajneesh Malhotra, Céline Dumont
Software Mentions: 4
Published: about 6 years ago
10.1038/s12276-021-00559-1
Practical prediction model of the clinical response to programmed death-ligand 1 inhibitors in advanced gastric cancerCited by: 9
Author(s): Myung‐Giun Noh, Young‐In Yoon, Gihyeon Kim, Hyun Kim, Eulgi Lee, Yeongmin Kim, Chang-Ho Park, Kyung‐Hwa Lee, Hansoo Park
Software Mentions: 4
Published: almost 4 years ago
10.1186/s12920-020-00820-y
Mutational profiling of micro-dissected pre-malignant lesions from archived specimensCited by: 4
Author(s): Daniela Nachmanson, J. S. Steward, Huazhen Yao, Adam Officer, Eliza Jeong, Thomas J. O’Keefe, Farnaz Hasteh, Kristen Jepsen, Gillian L. Hirst, Laura J. Esserman, Alexander D. Borowsky, Olivier Harismendy
Software Mentions: 4
Published: about 4 years ago
10.1186/s40168-019-0650-5
Species-specific enhancement of enterohemorrhagic E. coli pathogenesis mediated by microbiome metabolitesCited by: 93
Author(s): Alessio Tovaglieri, Alexandra Sontheimer-Phelps, Annelies Geirnaert, Rachelle Prantil‐Baun, Diogo M. Camacho, David B. Chou, Hossein Baharvand, Tomás de Wouters, Magdalena Kasendra, Michael Super, Mark Cartwright, Camilla A. Richmond, David T. Breault, Christophe Lacroix, Donald E. Ingber
Software Mentions: 4
Published: over 5 years ago
10.1038/s41598-021-94292-4
Prevalence of cancer susceptibility variants in patients with multiple Lynch syndrome related cancersCited by: 7
Author(s): Yoon Young Choi, Su‐Jin Shin, Jae Eun Lee, Lisa Madlensky, Seung Tae Lee, Ji Soo Park, Jeong-Hyeon Jo, Hyun Ki Kim, Daniela Nachmanson, Xiaojun Xu, Sung Hoon Noh, Jae‐Ho Cheong, Olivier Harismendy
Software Mentions: 4
Published: over 3 years ago
10.1038/srep14283
SeqMule: automated pipeline for analysis of human exome/genome sequencing dataCited by: 56
Author(s): Yunfei Guo, Xiaolei Ding, Yufeng Shen, Gholson J. Lyon, Kai Wang
Software Mentions: 3
Published: about 9 years ago
10.1186/s12859-017-1747-0
Investigating reproducibility and tracking provenance – A genomic workflow case studyCited by: 56
Author(s): Sehrish Kanwal, Farah Zaib Khan, Andrew Lonie, Richard O. Sinnott
Software Mentions: 3
Published: over 7 years ago
10.1186/s12859-018-2440-7
Comparing the performance of selected variant callers using synthetic data and genome segmentationCited by: 35
Author(s): Xiaopeng Bian, Bin Zhu, Mingyi Wang, Ying Hu, Qingrong Chen, Cu Nguyen, Belynda Hicks, Daoud Meerzaman
Software Mentions: 3
Published: about 6 years ago
10.1186/s12864-020-07224-3
Red panda: a novel method for detecting variants in single-cell RNA sequencingCited by: 0
Author(s): Adam Cornish, Shrabasti Roychoudhury, Krishna Sarma, Suravi Pramanik, Kishor K. Bhakat, Andrew T. Dudley, Nitish K. Mishra, Chittibabu Guda
Software Mentions: 3
Published: almost 4 years ago
10.1371/journal.pone.0248886
Detection of new drivers of frequent B-cell lymphoid neoplasms using an integrated analysis of whole genomesCited by: 11
Author(s): Adrián Mosquera Orgueira, Roi Ferreiro Ferro, José Ángel Díaz Arias, Cristina Santos, Beatriz Antelo Rodríguez, Laura Bao Pérez, Natalia Alonso Vence, Ággeles Bendaña López, Ayelén Melisa Blanco, Paula Melero Valentín, And Res Peleteiro Raindo, Marcos Pérez López, Manuel Mateo Pérez Encinas, Marta Sonia González Pérez, Marianela Rodríguez, José Luis Bello López
Software Mentions: 3
Published: over 3 years ago
10.3390/cancers13061340
Detection of Rare Germline Variants in the Genomes of Patients with B-Cell NeoplasmsCited by: 9
Author(s): Adrián Mosquera Orgueira, Marcos Pérez López, Andrés Peleteiro Raíndo, José Ángel Díaz Arias, Beatriz Antelo Rodríguez, Laura Bao Pérez, Natalia Alonso Vence, Ángeles Bendaña López, Ayelén Melisa Blanco, Paula Melero Valentín, Roi Ferreiro Ferro, Cristina Santos, Marianela Rodríguez, Marta Sonia González Pérez, Manuel Pérez‐Encinas, José Luis Bello López
Software Mentions: 3
Published: over 3 years ago
10.12688/f1000research.18142.2
Visualization of the small RNA transcriptome using seqclusterVizCited by: 6
Author(s): Lorena Pantano, Francisco Pantano, Eulàlia Martı́, Shannan Ho Sui
Software Mentions: 3
Published: over 5 years ago
10.3389/fonc.2019.01525
Involvement of Glutathione Depletion in Selective Cytotoxicity of Oridonin to p53-Mutant Esophageal Squamous Carcinoma CellsCited by: 19
Author(s): Yinchao Li, Nana Li, Jianxiang Shi, Tanzeel Ahmed, Hong‐Min Liu, Guo Liang Jiang, Wenxue Tang, Yongjun Guo, Qi Zhang
Software Mentions: 3
Published: almost 5 years ago
10.1186/s13075-018-1702-0
Cytokine production by activated plasmacytoid dendritic cells and natural killer cells is suppressed by an IRAK4 inhibitorCited by: 38
Author(s): Karin Hjorton, Niklas Hagberg, Elisabeth Israelsson, Lisa Jinton, Olof Berggren, Johanna K. Sandling, Kristofer Thörn, John Mo, Maija‐Leena Eloranta, Lars Rönnblom
Software Mentions: 3
Published: about 6 years ago
10.1038/s41598-018-21727-w
Bronchial extracellular matrix from COPD patients induces altered gene expression in repopulated primary human bronchial epithelial cellsCited by: 32
Author(s): Ulf Hedström, Oskar Hällgren, Lisa Öberg, Amy DeMicco, Outi Vaarala, Gunilla Westergren‐Thorsson, Xin Zhou
Software Mentions: 3
Published: over 6 years ago
10.3389/fnagi.2018.00155
Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgersCited by: 19
Author(s): Matthew J. Huentelman, Ignazio S. Piras, Ashley L. Siniard, Matthew De Both, Ryan Richholt, Chris Balak, Pouya Jamshidi, Eileen H. Bigio, Sandra Weıntraub, Emmaleigh Loyer, Marek-Marsel Mesulam, Changiz Geula, Emily Rogalskı
Software Mentions: 2
Published: over 6 years ago
10.1371/journal.pone.0132868
elPrep: High-Performance Preparation of Sequence Alignment/Map Files for Variant CallingCited by: 23
Author(s): Charlotte Herzeel, Pascal Costanza, Dries Decap, Jan Fostier, Joke Reumers
Software Mentions: 2
Published: over 9 years ago
10.1007/s00109-019-01792-y
Prospect and challenge of detecting dynamic gene copy number increases in stem cells by whole genome sequencingCited by: 2
Author(s): Ulrike Fischer, Christina Backes, Tobias Fehlmann, Valentina Galata, Andreas Keller, Eckart Meese
Software Mentions: 2
Published: over 5 years ago
10.1016/j.dib.2019.104022
Data on somatic mutations obtained by whole exome sequencing of FFPE tissue samples from Russian patients with prostate cancerCited by: 0
Author(s): Anastasia S. Nikitina, Е. И. Шарова, S. A. Danilenko, Oksana V. Selezneva, Liubov O. Skorodumova, Aleksandra V Kanygina, Konstantin Babalyan, A.O. Vasiliev, А. В. Говоров, E. A. Prilepskaya, Dmitry Pushkar, Elena S. Kostryukova, Edward V. Generozov
Software Mentions: 1
Published: over 5 years ago
10.1038/s41598-020-59243-5
Novel Mutation Hotspots within Non-Coding Regulatory Regions of the Chronic Lymphocytic Leukemia GenomeCited by: 4
Author(s): Adrián Mosquera Orgueira, Beatriz Antelo, José Ángel Díaz Arias, Nicolas Varela, Natalia Alonso Vence, Marta Sonia González Pérez, José Luis Bello López
Software Mentions: 1
Published: almost 5 years ago
10.1038/s41598-021-99347-0
Enhancing adoptive CD8 T cell therapy by systemic delivery of tumor associated antigensCited by: 5
Author(s): Ditte Jæhger, Mie Linder Hübbe, Martin Kisha Kræmer, Gael Clergeaud, André Vidas Olsen, Camilla Stavnsbjerg, Mette N. Wiinholt, Andreas Kjær, Jonas Rosager Henriksen, Anders Elias Hansen, Thomas Lars Andresen
Software Mentions: 1
Published: about 3 years ago
10.1093/jncics/pkab028
Preexisting Somatic Mutations of Estrogen Receptor Alpha (<i>ESR1</i>) in Early-Stage Primary Breast CancerCited by: 15
Author(s): Malin Dahlgren, Anthony George, Christian Brueffer, Sergii Gladchuk, Yilun Chen, Johan Vallon‐Christersson, Cecilia Hegardt, Jari Häkkinen, Lisa Rydén, Martin Malmberg, Christer Larsson, Sofia K. Gruvberger-Saal, Anna Ehinger, Niklas Loman, Åke Borg, Lao H. Saal
Software Mentions: 1
Published: over 3 years ago
10.1186/s13073-015-0191-x
Cpipe: a shared variant detection pipeline designed for diagnostic settingsCited by: 75
Author(s): Simon Sadedin, Harriet Dashnow, Paul James, Melanie Bahlo, Denis C. Bauer, Andrew Lonie, Sebastian Lunke, Ivan Macciocca, Jason P. Ross, Kirby Siemering, Zornitza Stark, Susan White, Graham R. Taylor, Clara Gaff, Alicia Oshlack, Natalie Thorne
Software Mentions: 1
Published: over 9 years ago
10.3389/fgene.2021.643546
High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation SequencingCited by: 5
Author(s): Sen Zhang, Hongen Xu, Yongan Tian, Danhua Liu, Xinyue Hou, Beiping Zeng, Bei Chen, Huanfei Liu, Ruijun Li, Xiaohua Li, Bin Zuo, Ryan W. Tang, Wenxue Tang
Software Mentions: 1
Published: over 3 years ago
10.3390/genes12040484
Novel GRHL2 Gene Variant Associated with Hearing Loss: A Case Report and Review of the LiteratureCited by: 2
Author(s): Katarina Trebušak Podkrajšek, Tine Tesovnik, Nina Božanić Urbančič, Saba Battelino
Software Mentions: 1
Published: over 3 years ago
10.1038/srep20768
Genomic study of the Ket: a Paleo-Eskimo-related ethnic group with significant ancient North Eurasian ancestryCited by: 47
Author(s): Pavel Flegontov, Piya Changmai, Anastassiya Zidkova, Maria D. Logacheva, N. Ezgi Altınışık, Olga Flegontova, Mikhail S. Gelfand, Evgeny S. Gerasimov, Ekaterina E. Khrameeva, Olga P. Konovalova, Tatyana V. Neretina, Yuri Nikolsky, George Starostin, Vita Stepanova, Igor V. Travinsky, Martin Tříska, Petr Tříska, Tatiana V. Tatarinova
Software Mentions: 1
Published: almost 9 years ago
10.1186/s12907-015-0004-6
A reliable method for the detection of BRCA1 and BRCA2 mutations in fixed tumour tissue utilising multiplex PCR-based targeted next generation sequencingCited by: 47
Author(s): Gillian Ellison, Shuwen Huang, T. Hedley Carr, Andrew Wallace, Miika J. Ahdesmäki, Sanjeev S. Bhaskar, John Mills
Software Mentions: 1
Published: over 9 years ago