DNA copy number profiling using single-cell sequencing (Q38979864)

8 September 2017

title

DNA copy number profiling using single-cell sequencing (English)

1 reference

8 September 2017

Xuefeng Wang

1

1 reference

8 September 2017

Hao Chen

series ordinal

2

1 reference

8 September 2017

Nancy R Zhang

series ordinal

3

1 reference

8 September 2017

publication date

4 February 2017

1 reference

Briefings in Bioinformatics

8 September 2017

published in

1 reference

Tumour evolution inferred by single-cell sequencing

8 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Single-cell RNA-seq supports a developmental hierarchy in human oligodendroglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Allele-specific copy number profiling by next-generation DNA sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Genome-wide copy number analysis of single cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Estimating optimal window size for analysis of low-coverage next-generation sequence data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

A faster circular binary segmentation algorithm for the analysis of array CGH data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

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%2FBIB%2FBBX004

Integrating copy number polymorphisms into array CGH analysis using a robust HMM.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Single-cell genome sequencing: current state of the science

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Single-Cell Whole-Genome Amplification and Sequencing: Methodology and Applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Interactive analysis and assessment of single-cell copy-number variations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Assessment of megabase-scale somatic copy number variation using single-cell sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

A single cell level based method for copy number variation analysis by low coverage massively parallel sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Absolute quantification of somatic DNA alterations in human cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Global copy number profiling of cancer genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBX004

Cancer genomics: one cell at a time

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28159966

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Method of the Year 2013

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28159966

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BIB/BBX004

1 reference

8 September 2017

DBLP publication ID

journals/bib/WangCZ18

1 reference

DBLP Dataset 2021-01-02

28 January 2021

PMC publication ID

6171490

0 references

1 reference