(Q33775428)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21170042%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

title

Haplotype-resolved genome sequencing of a Gujarati Indian individual (English)

1 reference

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18 January 2020

0 references

6

1 reference

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18 January 2020

Can Alkan

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21170042%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Jay Shendure

11

1 reference

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18 January 2020

Jacob O Kitzman

1

1 reference

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18 January 2020

10

Evan E Eichler

1 reference

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18 January 2020

4

Joseph B Hiatt

1 reference

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18 January 2020

9

Ruolan Qiu

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21170042%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

author name string

Alexandra P Mackenzie

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21170042%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Andrew Adey

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21170042%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Rupali P Patwardhan

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21170042%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Sarah B Ng

7

1 reference

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18 January 2020

publication date

19 December 2010

1 reference

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18 January 2020

1 reference

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18 January 2020

volume

29

1 reference

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18 January 2020

issue

1

1 reference

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18 January 2020

page(s)

59-63

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21170042%20AND%20SRC:MED&resulttype=core&format=json

Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition

18 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

A map of human genome variation from population-scale sequencing

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Allele-specific DNA methylation: beyond imprinting

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Integrating common and rare genetic variation in diverse human populations

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Assembly of large genomes using second-generation sequencing

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

A Draft Sequence of the Neandertal Genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Direct determination of molecular haplotypes by chromosome microdissection.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Building the sequence map of the human pan-genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Exome sequencing identifies the cause of a mendelian disorder

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Reconstructing Indian population history

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Personalized copy number and segmental duplication maps using next-generation sequencing.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Targeted capture and massively parallel sequencing of 12 human exomes

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Fast and accurate short read alignment with Burrows-Wheeler transform

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Evolutionary toggling of the MAPT 17q21.31 inversion region

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

The diploid genome sequence of an Asian individual

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Next-generation DNA sequencing

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

An MCMC algorithm for haplotype assembly from whole-genome sequence data

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Mapping and sequencing of structural variation from eight human genomes

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Paired-end mapping reveals extensive structural variation in the human genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

The diploid genome sequence of an individual human

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Diploid genome reconstruction of Ciona intestinalis and comparative analysis with Ciona savignyi

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Initial sequencing and analysis of the human genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3116788

HapCUT: an efficient and accurate algorithm for the haplotype assembly problem

4 July 2018

1 reference

Targeted, haplotype-resolved resequencing of long segments of the human genome

21 January 2018

1 reference

Diversity of human copy number variation and multicopy genes

21 January 2018

1 reference

Velvet: algorithms for de novo short read assembly using de Bruijn graphs

21 January 2018

1 reference

Human genome: Genomes by the thousand

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1038/NBT.1740

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21170042%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21170042%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

PubMed publication ID

21170042

1 reference