SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies (Q34139473)

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14 February 2020

title

SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies (English)

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14 February 2020

2

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14 February 2020

Richard W. Morris

6

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14 February 2020

author name string

E R Martin

1

1 reference

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14 February 2020

M A Schmidt

3

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14 February 2020

E H Powell

4

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14 February 2020

S Zuchner

5

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14 February 2020

language of work or name

English

0 references

publication date

21 September 2010

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14 February 2020

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14 February 2020

volume

26

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14 February 2020

issue

22

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14 February 2020

page(s)

2803-2810

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Exome sequencing of a multigenerational human pedigree

14 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

Exome sequencing identifies the cause of a mendelian disorder

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

Massively parallel sequencing: the next big thing in genetic medicine

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

Multiplex padlock targeted sequencing reveals human hypermutable CpG variations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

SNP detection for massively parallel whole-genome resequencing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

Mapping short DNA sequencing reads and calling variants using mapping quality scores

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

Simple and efficient analysis of disease association with missing genotype data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

Multiplex amplification of large sets of human exons

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

A new multipoint method for genome-wide association studies by imputation of genotypes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

Score tests for association between traits and haplotypes when linkage phase is ambiguous

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971572

10.1093/BIOINFORMATICS/BTQ526

5 July 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861027%20AND%20SRC:MED&resulttype=core&format=json

journals/bioinformatics/MartinKSPZM10

14 February 2020

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861027%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference