(Q33820514)

29 July 2017

title

Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm (English)

1 reference

high-throughput sequencing

29 July 2017

main subject

1 reference

Matteo Benelli

2

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Alberto Magi

object named as

Alberto Magi

1

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author name string

Seungtai Yoon

3

1 reference

29 July 2017

Franco Roviello

4

1 reference

29 July 2017

Francesca Torricelli

5

1 reference

29 July 2017

language of work or name

English

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publication date

14 February 2011

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29 July 2017

published in

Nucleic Acids Research

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29 July 2017

volume

39

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29 July 2017

issue

10

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29 July 2017

page(s)

e65

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Creative Commons Attribution-NonCommercial 2.5 Generic

29 July 2017

copyright license

start time

4 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Genome variation discovery with high-throughput sequencing data

4 July 2018

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A shifting level model algorithm that identifies aberrations in array-CGH data

4 July 2018

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Computational methods for discovering structural variation with next-generation sequencing

4 July 2018

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Sensitive and accurate detection of copy number variants using read depth of coverage

4 July 2018

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High-resolution mapping of copy-number alterations with massively parallel sequencing

4 July 2018

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4 July 2018

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Accurate whole human genome sequencing using reversible terminator chemistry

4 July 2018

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Systematic assessment of copy number variant detection via genome-wide SNP genotyping

4 July 2018

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Integrated detection and population-genetic analysis of SNPs and copy number variation

4 July 2018

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Mapping and sequencing of structural variation from eight human genomes

4 July 2018

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Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

4 July 2018

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Copy-number variation and association studies of human disease

4 July 2018

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Global variation in copy number in the human genome

4 July 2018

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Bias of selection on human copy-number variants

4 July 2018

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Structural variation in the human genome

4 July 2018

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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

4 July 2018

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4 July 2018

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

4 July 2018

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Analysis of array CGH data: from signal ratio to gain and loss of DNA regions

4 July 2018

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Detection of large-scale variation in the human genome

4 July 2018

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4 July 2018

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alpha-Synuclein locus triplication causes Parkinson's disease

4 July 2018

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End-sequence profiling: sequence-based analysis of aberrant genomes

4 July 2018

1 reference

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Reconstructing tumor genome architectures

4 July 2018

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Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKR068

A tutorial on hidden Markov models and selected applications in speech recognition

21 January 2018

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https://api.crossref.org/works/10.1093%2FNAR%2FGKR068

CGHcall: calling aberrations for array CGH tumor profiles.

21 January 2018

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https://api.crossref.org/works/10.1093%2FNAR%2FGKR068

21 January 2018

Identifiers

DOI

10.1093/NAR/GKR068

1 reference

29 July 2017

0 references

1 reference

29 July 2017

1 reference