(Q35795078)

10 August 2017

title

Efficient study design for next generation sequencing (English)

1 reference

10 August 2017

3

Meredith Yeager

0 references

Stephen Chanock

series ordinal

4

object named as

Stephen Chanock

1 reference

10 August 2017

5

Nilanjan Chatterjee

1 reference

10 August 2017

2

Kevin Jacobs

1 reference

10 August 2017

Joshua Sampson

1

1 reference

10 August 2017

publication date

1 May 2011

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10 August 2017

1 reference

10 August 2017

volume

35

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10 August 2017

issue

4

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10 August 2017

page(s)

269-277

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A map of human genome variation from population-scale sequencing

10 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Characterization of missing human genome sequences and copy-number polymorphic insertions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Accurate detection and genotyping of SNPs utilizing population sequencing data

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Sequencing technologies - the next generation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Exome sequencing identifies the cause of a mendelian disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Bioinformatics approaches for genomics and post genomics applications of next-generation sequencing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

The theory of discovering rare variants via DNA sequencing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Statistical aspects of discerning indel-type structural variation via DNA sequence alignment

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Discovery of rare variants via sequencing: implications for the design of complex trait association studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Evaluation of next generation sequencing platforms for population targeted sequencing studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

The diploid genome sequence of an Asian individual

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Next-generation DNA sequencing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Estimating coverage and power for genetic association studies using near-complete variation data

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Aspects of coverage in medical DNA sequencing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Structural variation in the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Extension of Lander-Waterman theory for sequencing filtered DNA libraries.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Generalized gap model for bacterial artificial chromosome clone fingerprint mapping and shotgun sequencing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Genomic mapping by fingerprinting random clones: a mathematical analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3291790

Pyrobayes: an improved base caller for SNP discovery in pyrosequences.

12 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.20575

Modeling the feasibility of whole genome shotgun sequencing using a pairwise end strategy.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.20575

1000 Genomes Project promises closer look at variation in human genome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21370254

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

DNA sequencing. A plan to capture human diversity in 1000 genomes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21370254

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/21370254

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/GEPI.20575

1 reference

10 August 2017

1 reference

10 August 2017

1 reference