(Q36642284)

15 August 2017

Interactive analysis and assessment of single-cell copy-number variations (English)

1 reference

15 August 2017

8

1 reference

15 August 2017

7

Michael Wigler

1 reference

15 August 2017

Tyler Garvin

1

1 reference

15 August 2017

Robert Aboukhalil

2

1 reference

15 August 2017

Jude Kendall

3

1 reference

15 August 2017

Timour Baslan

4

1 reference

15 August 2017

Gurinder S Atwal

5

1 reference

15 August 2017

James Hicks

6

1 reference

15 August 2017

7 September 2015

1 reference

15 August 2017

1 reference

15 August 2017

12

1 reference

15 August 2017

11

1 reference

15 August 2017

1058-1060

1 reference

Comparison of multiple displacement amplification (MDA) and multiple annealing and looping-based amplification cycles (MALBAC) in single-cell sequencing

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Cancer genomics: one cell at a time

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

A quantitative comparison of single-cell whole genome amplification methods

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Reproducible copy number variation patterns among single circulating tumor cells of lung cancer patients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Mosaic copy number variation in human neurons

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Single-cell sequencing-based technologies will revolutionize whole-organism science

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Characterizing and measuring bias in sequence data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

The future is now: single-cell genomics of bacteria and archaea

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Probing meiotic recombination and aneuploidy of single sperm cells by whole-genome sequencing

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Genome-wide detection of single-nucleotide and copy-number variations of a single human cell

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Genome-wide single-cell analysis of recombination activity and de novo mutation rates in human sperm

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Genome-wide copy number analysis of single cells.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Direct, genome-wide assessment of DNA mutations in single cells.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Tumour evolution inferred by single-cell sequencing

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Genome structural variation discovery and genotyping

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

jsPhyloSVG: a javascript library for visualizing interactive and vector-based phylogenetic trees on the web

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Inferring tumor progression from genomic heterogeneity

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Copy number variants, diseases and gene expression

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Broad applications of single-cell nucleic acid analysis in biomedical research.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4775251

Genome analyses of single human oocytes

20 September 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3578

Single-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3578

Sequencing of isolated sperm cells for direct haplotyping of a human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3578

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3578

Optimizing sparse sequencing of single cells for highly multiplex copy number profiling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3578

LOWESS: A Program for Smoothing Scatterplots by Robust Locally Weighted Regression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3578

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3578

Modeling genome coverage in single-cell sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3578

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3578

21 January 2018

Identifiers

DOI

10.1038/NMETH.3578

1 reference

Dimensions Publication ID

15 August 2017

0 references

1 reference

15 August 2017

PubMed publication ID

26344043

1 reference