(Q48182929)

9 February 2018

title

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

1 reference

9 February 2018

main subject

whole genome duplication

1 reference

1

1 reference

9 February 2018

Johan T Den Dunnen

object named as

Johan T Den Dunnen

5

0 references

Anthony J Brookes

6

object named as

Anthony J Brookes

1 reference

9 February 2018

author name string

Stefan J White

2

1 reference

9 February 2018

Susanna Potter

3

1 reference

9 February 2018

Evan E Eichler

4

1 reference

9 February 2018

language of work or name

English

0 references

publication date

11 July 2004

1 reference

9 February 2018

published in

Nature Genetics

1 reference

9 February 2018

volume

36

1 reference

9 February 2018

issue

8

1 reference

9 February 2018

page(s)

861-866

1 reference

9 February 2018

The Sequence of the Human Genome

cites work

1 reference

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

Recent segmental duplications in the human genome

21 January 2018

1 reference

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

21 January 2018

1 reference

Whole-genome shotgun assembly and comparison of human genome assemblies

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Gene conversion homogenizes the CMT1A paralogous repeats

21 January 2018

1 reference

Are 100,000 "SNPs" useless?

21 January 2018

1 reference

Asymmetric sequence divergence of duplicate genes

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Interspersed repeats and other mementos of transposable elements in mammalian genomes

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

dbSNP: the NCBI database of genetic variation

21 January 2018

1 reference

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Variation is the spice of life

21 January 2018

1 reference

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

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG1401

1 reference

9 February 2018

1 reference

9 February 2018