(Q30440990)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24681819%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

title

Non-random DNA fragmentation in next-generation sequencing (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24681819%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

1

1 reference

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12 March 2020

Nina Oparina

6

1 reference

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12 March 2020

author name string

Irina A Il'icheva

2

1 reference

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12 March 2020

Dmitry Yu Nechipurenko

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24681819%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

Larisa A Panchenko

4

1 reference

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12 March 2020

Mingian V Khodikov

5

1 reference

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12 March 2020

Robert V Polozov

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24681819%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

Yury D Nechipurenko

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24681819%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

Sergei L Grokhovsky

9

1 reference

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12 March 2020

language of work or name

English

0 references

publication date

31 March 2014

1 reference

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12 March 2020

1 reference

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12 March 2020

volume

4

1 reference

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12 March 2020

page(s)

4532

1 reference

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Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

12 March 2020

copyright license

start time

31 March 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Long insert whole genome sequencing for copy number variant and translocation detection

1 reference

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Reprever: resolving low-copy duplicated sequences using template driven assembly

20 June 2018

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Effects of GC bias in next-generation-sequencing data on de novo genome assembly

20 June 2018

1 reference

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Systematic biases in DNA copy number originate from isolation procedures

20 June 2018

1 reference

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Probing DNA shape and methylation state on a genomic scale with DNase I.

20 June 2018

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Probabilistic error correction for RNA sequencing

20 June 2018

1 reference

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The effect of strand bias in Illumina short-read sequencing data

20 June 2018

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Genome-wide patterns of natural variation reveal strong selective sweeps and ongoing genomic conflict in Drosophila mauritiana

20 June 2018

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High-throughput bacterial genome sequencing: an embarrassment of choice, a world of opportunity.

20 June 2018

1 reference

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Summarizing and correcting the GC content bias in high-throughput sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Systematic comparison of three methods for fragmentation of long-range PCR products for next generation sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Repetitive DNA and next-generation sequencing: computational challenges and solutions

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Systematic bias in high-throughput sequencing data and its correction by BEADS.

20 June 2018

1 reference

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Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Detection and removal of biases in the analysis of next-generation sequencing reads

20 June 2018

1 reference

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Mapping copy number variation by population-scale genome sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Sequence-specific ultrasonic cleavage of DNA

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Overcoming bias and systematic errors in next generation sequencing data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

A map of human genome variation from population-scale sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Detecting copy number variation with mated short reads

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Biases in Illumina transcriptome sequencing caused by random hexamer priming

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Sequencing technologies - the next generation

20 June 2018

1 reference

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

20 June 2018

1 reference

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Mapping accessible chromatin regions using Sono-Seq

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Amplification-free Illumina sequencing-library preparation facilitates improved mapping and assembly of (G+C)-biased genomes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Local DNA topography correlates with functional noncoding regions of the human genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

Next-generation DNA sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

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

20 June 2018

1 reference

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DNA transposons and the evolution of eukaryotic genomes

20 June 2018

1 reference

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PCR bias in amplification of androgen receptor alleles, a trinucleotide repeat marker used in clonality studies

20 June 2018

1 reference

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A strategy of DNA sequencing employing computer programs

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3970190

20 June 2018

Single-cell epigenetics

1 reference

The dynamics of genome replication using deep sequencing.

21 January 2018

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DNA acts as a nucleation site for transient cavitation in the ultrasonic nebulizer.

21 January 2018

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Ultrasonic cleavage of nicked DNA.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1038/SREP04532

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24681819%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

12 March 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24681819%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24681819%20AND%20SRC:MED&resulttype=core&format=json