You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Copy file name to clipboardExpand all lines: README.md
+2Lines changed: 2 additions & 0 deletions
Display the source diff
Display the rich diff
Original file line number
Diff line number
Diff line change
@@ -1,5 +1,7 @@
1
1
# 🧬 gnomAD Python API (Batch Script)
2
2
3
+

4
+
3
5
## :hash: What is *gnomAD* and the purpose of this script?
4
6
[gnomAD (The Genome Aggregation Database)](http://gnomad.broadinstitute.org/) is aggregation of thousands of exomes and genomes human sequencing studies. Also, gnomAD consortium annotates the variants with allelic frequency in genomes and exomes.
5
7
**Here**, this batch script is able to search the genes or transcripts of your interest and retrieve variant data from the database via [gnomAD backend API](https://gnomad.broadinstitute.org/api) that based on GraphQL query language.
0 commit comments