(Q37971383)

26 August 2017

Read count approach for DNA copy number variants detection (English)

1 reference

26 August 2017

3

Tommaso Pippucci

1 reference

26 August 2017

Alberto Magi

1

1 reference

26 August 2017

Lorenzo Tattini

series ordinal

2

1 reference

26 August 2017

Francesca Torricelli

series ordinal

4

1 reference

26 August 2017

Matteo Benelli

series ordinal

5

1 reference

26 August 2017

language of work or name

English

0 references

publication date

23 December 2011

1 reference

26 August 2017

1 reference

26 August 2017

28

1 reference

26 August 2017

470-478

1 reference

26 August 2017

4

1 reference

CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

26 August 2017

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Genome structural variation discovery and genotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

A very fast and accurate method for calling aberrations in array-CGH data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Accurate whole human genome sequencing using reversible terminator chemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Origins and functional impact of copy number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Genome variation discovery with high-throughput sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

A map of human genome variation from population-scale sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Evaluation of next generation sequencing platforms for population targeted sequencing studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Whole-genome sequencing and variant discovery in C. elegans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

CNAseg--a novel framework for identification of copy number changes in cancer from second-generation sequencing data.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Mapping and sequencing of structural variation from eight human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

The diploid genome sequence of an individual human

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

The Sequence Alignment/Map format and SAMtools

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Computational methods for discovering structural variation with next-generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

ReadDepth: a parallel R package for detecting copy number alterations from short sequencing reads

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

An initial map of insertion and deletion (INDEL) variation in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Towards a comprehensive structural variation map of an individual human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

Fine-scale structural variation of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

CGHcall: calling aberrations for array CGH tumor profiles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

The complete genome of an individual by massively parallel DNA sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

CNV-seq, a new method to detect copy number variation using high-throughput sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR707

10.1093/BIOINFORMATICS/BTR707

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/MagiTPTB12

26 August 2017

1 reference

DBLP Dataset 2021-01-02

release_eawx5jvlv5ckfae5yrr3lnhyr4

28 January 2021

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/eawx5jvlv5ckfae5yrr3lnhyr4

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference