CORE
🇺🇦Â
 make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Filters
1 research outputs found
exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels
Author
1000 Genomes Project Consortium
Adzhubei
+48Â more
B. Maranhao
Cideciyan
Cukras
DePristo
Ensembl
Ferrer-Costa
forge
Friedman
G.A. Silva
Gonzalez-Fernandez
Herz
I. of Medical Genetics in Cardiff
International HapMap 3 Consortium
J.F. Hejtmancik
J.L. Duncan
J.R. Heckenlively
Jeon
Joernvall
K.E. Branham
Kaul
Kaul
Kozomara
Kumar
L. for the Molecular Diagnosis of Inherited Eye Diseases
Le Quesne Stabej
Li
Li
M.A. Naeem
McGee
Nakamura
NCBI
NCBI
Niwa
P. Biswas
P.L. Lee
R. Ayyagari
Reese
S. Riazuddin
S.A. Riazuddin
S.N. Khan
Schwarz
Seelow
Tavtigian
Toomes
UCSC
W. NHLBI GO Exome Sequencing Project (ESP)
Wang
Yamamoto
Publication venue
'Elsevier BV'
Publication date
Field of study
No full text
Crossref