Accurate and reliable high-throughput detection of copy number variation in the human genome (Q35173713)

6 August 2017

Accurate and reliable high-throughput detection of copy number variation in the human genome (English)

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6 August 2017

2

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6 August 2017

22

Cordelia Langford

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6 August 2017

James Larkin

14

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Rachel E Rigby

object named as

Rachel E Rigby

19

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Stephen W. Scherer

24

object named as

Stephen W Scherer

1 reference

6 August 2017

Armand Valsesia

21

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Lars Feuk

10

object named as

Lars Feuk

1 reference

6 August 2017

Heike Fiegler

1

1 reference

6 August 2017

Dan Andrews

3

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6 August 2017

Carol Scott

4

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6 August 2017

Robert Andrews

5

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6 August 2017

Carol Carder

6

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6 August 2017

Richard Clark

7

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6 August 2017

Oliver Dovey

8

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6 August 2017

Peter Ellis

9

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6 August 2017

Lisa French

11

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6 August 2017

Paul Hunt

12

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6 August 2017

Dimitrios Kalaitzopoulos

13

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6 August 2017

Lyndal Montgomery

15

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6 August 2017

George H Perry

16

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6 August 2017

Bob W Plumb

17

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6 August 2017

Keith Porter

18

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6 August 2017

Diane Rigler

20

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6 August 2017

Sean J Humphray

23

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6 August 2017

Charles Lee

25

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6 August 2017

Matthew E Hurles

26

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6 August 2017

Nigel P Carter

27

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6 August 2017

22 November 2006

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6 August 2017

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16

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12

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6 August 2017

1566-1574

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Hotspots for copy number variation in chimpanzees and humans

6 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

A genome-wide, end-sequenced 129Sv BAC library resource for targeting vector construction

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

A genome-wide survey of structural variation between human and chimpanzee

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

Segmental duplications and copy-number 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=1665640

Fine-scale structural variation 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=1665640

Circular binary segmentation for the analysis of array-based DNA copy number data

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

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=1665640

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=1665640

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

Contiguation of bacterial clones

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

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=1665640

Contigs built with fingerprints, markers, and FPC V4.7.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

High throughput fingerprint analysis of large-insert clones

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

Identification of common molecular subsequences

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1665640

A high-resolution survey of deletion polymorphism in the human genome

13 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17122085

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17122085

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A tiling resolution DNA microarray with complete coverage of the human genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17122085

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Global variation in copy number in the human genome

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/NATURE05329

Identifiers

DOI

10.1101/GR.5630906

1 reference

6 August 2017

1 reference

6 August 2017

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