(Q35911639)

11 August 2017

The ICR1000 UK exome series: a resource of gene variation in an outbred population (English)

1 reference

11 August 2017

12

1 reference

11 August 2017

Emma Poyastro-Pearson

object named as

Emma Ramsay

5

0 references

Shazia Mahamdallie

7

object named as

Shazia Mahamdallie

1 reference

11 August 2017

10

Ann Strydom

1 reference

11 August 2017

1

Elise Ruark

1 reference

11 August 2017

3

Anthony Renwick

1 reference

11 August 2017

Márton Münz

2

1 reference

11 August 2017

Matthew Clarke

4

1 reference

11 August 2017

Sandra Hanks

6

1 reference

11 August 2017

Anna Elliott

8

1 reference

11 August 2017

Sheila Seal

9

1 reference

11 August 2017

Lunter Gerton

11

1 reference

11 August 2017

22 September 2015

1 reference

11 August 2017

1 reference

11 August 2017

4

1 reference

11 August 2017

883

1 reference

Creative Commons Attribution 4.0 International

11 August 2017

start time

22 September 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

An integrated map of genetic variation from 1,092 human genomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

Evolution and functional impact of rare coding variation from deep sequencing of human exomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

A systematic survey of loss-of-function variants in human protein-coding genes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

The International HapMap Project

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

Large-scale whole-genome sequencing of the Icelandic population

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

Whole-genome sequence variation, population structure and demographic history of the Dutch population

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

A framework for variation discovery and genotyping using next-generation DNA sequencing data

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4706061

10.12688/F1000RESEARCH.7049.1

24 September 2018

Identifiers

DOI

1 reference

11 August 2017

1 reference

11 August 2017

1 reference