(Q36576540)

15 August 2017

Multiallelic Positions in the Human Genome: Challenges for Genetic Analyses (English)

1 reference

15 August 2017

9

Eric Boerwinkle

0 references

Tomasz Gambin

2

object named as

Tomasz Gambin

1 reference

15 August 2017

11

James R Lupski

1 reference

15 August 2017

8

Richard A Gibbs

1 reference

15 August 2017

6

Donna M Muzny

1 reference

15 August 2017

3

Shalini Jhangiani

1 reference

15 August 2017

Ian M Campbell

1

1 reference

15 August 2017

Megan L Grove

4

1 reference

15 August 2017

Narayanan Veeraraghavan

5

1 reference

15 August 2017

Chad A Shaw

7

1 reference

15 August 2017

Fuli Yu

10

1 reference

15 August 2017

language of work or name

1 reference

16 December 2015

1 reference

15 August 2017

1 reference

15 August 2017

37

1 reference

15 August 2017

3

1 reference

15 August 2017

231-234

1 reference

Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

Integrating common and rare genetic variation in diverse human populations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

A SNP discovery method to assess variant allele probability from next-generation resequencing data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

Segmental duplications: organization and impact within the current human genome project assembly

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

Deviations from Hardy-Weinberg proportions for multiple alleles under viability selection

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4752396

Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome

20 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FHUMU.22944

Shotgun sequence assembly and recent segmental duplications within the human genome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26670213

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/HUMU.22944

1 reference

15 August 2017

1 reference

15 August 2017

PubMed publication ID

26670213

1 reference