(Q35217155)

7 August 2017

title

Context-dependent individualization of nucleotides and virtual genomic hybridization allow the precise location of human SNPs (English)

1 reference

7 August 2017

2

Laura Gómez-Romero

1 reference

7 August 2017

Ximena Ibarra-Soria

3

1 reference

ORCID Public Data File 2021

author name string

José Reyes

1

1 reference

7 August 2017

Kim Palacios-Flores

4

1 reference

7 August 2017

Luis R Arriola

5

1 reference

7 August 2017

Alejandro Wences

6

1 reference

7 August 2017

Delfino García

7

1 reference

7 August 2017

Margareta Boege

8

1 reference

7 August 2017

Guillermo Dávila

9

1 reference

7 August 2017

Margarita Flores

10

1 reference

7 August 2017

Rafael Palacios

11

1 reference

7 August 2017

language of work or name

English

0 references

publication date

29 August 2011

1 reference

Proceedings of the National Academy of Sciences of the United States of America

7 August 2017

number of pages

6

1 reference

based on heuristic

inferred from page(s)

published in

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7 August 2017

volume

108

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7 August 2017

issue

37

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7 August 2017

page(s)

15294-15299

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Genome structural variation discovery and genotyping

7 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=3174668

Discovery and genotyping of genome structural polymorphism by sequencing on a population scale

13 July 2018

1 reference

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The uniqueome: a mappability resource for short-tag sequencing

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

A map of human genome variation from population-scale sequencing

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Galaxy: a web-based genome analysis tool for experimentalists

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

A highly annotated whole-genome sequence of a Korean individual

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Accurate whole human genome sequencing using reversible terminator chemistry

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

The complete genome of an individual by massively parallel DNA sequencing

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

A second generation human haplotype map of over 3.1 million SNPs

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

The diploid genome sequence of an individual human

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

A haplotype map of the human genome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Finishing the euchromatic sequence of the human genome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Detection of large-scale variation in the human genome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Large-scale copy number polymorphism in the human genome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

The UCSC Table Browser data retrieval tool

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Initial sequencing and analysis of the human genome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174668

Editorial expression of concern

13 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21876154

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.1112567108

1 reference

7 August 2017

0 references

1 reference

7 August 2017

1 reference