Paper
Paper
Search...
Search ResearchHub...
Ctrl+K
New
Home
Browse
Earn
Fund
RH Journal
Notebook
Lists
Leaderboard
RSC
USD
Changelog
Terms
Privacy
Issues
Docs
Support
Foundation
About
Comparing multi- and single-sample variant calls to impro... | ResearchHub
Paper
Paper
Search...
Search ResearchHub...
Ctrl+K
New
Home
Browse
Earn
Fund
RH Journal
Notebook
Lists
Leaderboard
RSC
USD
Changelog
Terms
Privacy
Issues
Docs
Support
Foundation
About
Comparing multi- and single-sample variant calls to improve variant call sets from deep coverage whole-genome sequencing data
0
Authors
Suyash Shringarpure
12 more
Suyash Shringarpure
•
Rasika Mathias
10 more
•
Margaret Taub
Published
September 30, 2016
Paper
Conversation
0
Reviews
0
Bounties
0
Sign in to comment
Add a comment...
Best
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Bioinformatics
Computer Science
Chemistry
Genomics
Show all topics
DOI
10.1101/078642
License
CC-BY-NC-ND
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Bioinformatics
Computer Science
Chemistry
Genomics
Show all topics
DOI
10.1101/078642
License
CC-BY-NC-ND
Other Formats
PDF
