Complex SNP-related sequence variation in segmental genome duplications (Q48182929)

9 February 2018

title

Complex SNP-related sequence variation in segmental genome duplications (English)

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main subject

whole genome duplication

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1

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Johan T Den Dunnen

object named as

Johan T Den Dunnen

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Anthony J Brookes

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object named as

Anthony J Brookes

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9 February 2018

author name string

Stefan J White

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Susanna Potter

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Evan E Eichler

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language of work or name

English

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publication date

11 July 2004

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9 February 2018

published in

Nature Genetics

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volume

36

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issue

8

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page(s)

861-866

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The Sequence of the Human Genome

cites work

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Initial sequencing and analysis of the human genome

21 January 2018

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Recent segmental duplications in the human genome

21 January 2018

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Segmental duplications: organization and impact within the current human genome project assembly

21 January 2018

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Whole-genome shotgun assembly and comparison of human genome assemblies

21 January 2018

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Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

21 January 2018

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Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome

21 January 2018

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Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence

21 January 2018

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

21 January 2018

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Single nucleotide polymorphisms (SNPs) that map to gaps in the human SNP map

21 January 2018

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Gene conversion homogenizes the CMT1A paralogous repeats

21 January 2018

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Are 100,000 "SNPs" useless?

21 January 2018

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Asymmetric sequence divergence of duplicate genes

21 January 2018

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Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation

21 January 2018

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Histopathological diagnosis of partial and complete hydatidiform mole in the first trimester of pregnancy

21 January 2018

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Interspersed repeats and other mementos of transposable elements in mammalian genomes

21 January 2018

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Intense and highly localized gene conversion activity in human meiotic crossover hot spots

21 January 2018

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Abundant gene conversion between arms of palindromes in human and ape Y chromosomes.

21 January 2018

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Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster

21 January 2018

1 reference

BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications

21 January 2018

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

21 January 2018

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Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

21 January 2018

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dbSNP: the NCBI database of genetic variation

21 January 2018

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21 January 2018

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DFold: PCR design that minimizes secondary structure and optimizes downstream genotyping applications

21 January 2018

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Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans

21 January 2018

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Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridization

21 January 2018

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Variation is the spice of life

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Two-color multiplex ligation-dependent probe amplification: Detecting genomic rearrangements in hereditary multiple exostoses

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG1401

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9 February 2018

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9 February 2018