An open API service providing mapping between scientific papers and software projects that are mentioned in them.

Papers: 10.1371/journal.pgen.1009803

https://doi.org/10.1371/journal.pgen.1009803

A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder

Cited by: 4
Author(s): Zineb Ammous, Lettie E Rawlins, Hannah Jones, Joseph S Leslie, Olivia Wenger, Ethan M. Scott, Jim Deline, Tom Herr, R. J. Evans, Angela Scheid, Joanna Kennedy, Barry A. Chioza, Ryan M. Ames, Harold E. Cross, Erik G. Puffenberger, Lorna W. Harries, Emma L. Baple, Andrew H. Crosby
Published: almost 4 years ago

Software Mentions 3

bioconductor: edgeR
Empirical Analysis of Digital Gene Expression Data in R
Papers that mentioned: 6,568
Very Likely Science (100)
cran: ExomeDepth
Calls Copy Number Variants from Targeted Sequence Data
Papers that mentioned: 112
Very Likely Science (75)
pypi: PACE
Data Quality of Experimental Data
Papers that mentioned: 13,779
Very Likely Science (90)