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
Complex Structural Variants Resolved by Short-Read and Lo... | 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
Complex Structural Variants Resolved by Short-Read and Long-Read Whole Genome Sequencing in Mendelian Disorders
0
Authors
Alba Sanchis-Juan
22 more
Alba Sanchis-Juan
•
Trevor Cole
20 more
•
Keren Carss
Published
March 14, 2018
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
Genomics
Genetics And Genomics
Genetics
Gene Duplication
Show all topics
DOI
10.1101/281683
License
cc-no
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genomics
Genetics And Genomics
Genetics
Gene Duplication
Show all topics
DOI
10.1101/281683
License
cc-no