Local alignment of two-base encoded DNA sequence (Q33464728)

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Language	Label	Description	Also known as
English	Local alignment of two-base encoded DNA sequence	scientific article

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instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

title

Local alignment of two-base encoded DNA sequence (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

main subject

sequence alignment

1 reference

based on heuristic

inferred from title

author

Stanley F Nelson

series ordinal

3

object named as

Stanley F Nelson

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

author name string

Nils Homer

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

Barry Merriman

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

publication date

9 June 2009

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

published in

BMC Bioinformatics

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stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

volume

10

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stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

page(s)

175

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

copyright license

Creative Commons Attribution 2.0 Generic

start time

9 June 2009

1 reference

stated in

April 2022 Public Data File from Crossref

copyright status

copyrighted

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stated in

April 2022 Public Data File from Crossref

cites work

SHRiMP: accurate mapping of short color-space reads

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PubMed Central

reference URL

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21 June 2018

Mapping short DNA sequencing reads and calling variants using mapping quality scores

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PubMed Central

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21 June 2018

SOAP: short oligonucleotide alignment program

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709925

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21 June 2018

The diploid genome sequence of an individual human

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709925

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21 June 2018

PatternHunter: faster and more sensitive homology search

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709925

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21 June 2018

BLAT—The BLAST-Like Alignment Tool

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709925

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21 June 2018

SSAHA: a fast search method for large DNA databases

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PubMed Central

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21 June 2018

Improvement of base-calling in multilane automated DNA sequencing by use of electrophoretic calibration standards, data linearization, and trace alignment

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709925

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21 June 2018

dbSNP: the NCBI database of genetic variation

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PubMed Central

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21 June 2018

Base-calling of automated sequencer traces using phred. II. Error probabilities

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PubMed Central

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21 June 2018

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

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PubMed Central

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21 June 2018

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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PubMed Central

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21 June 2018

Identification of common molecular subsequences

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709925

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21 June 2018

A general method applicable to the search for similarities in the amino acid sequence of two proteins

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21 June 2018

Optimal alignments in linear space

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709925

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21 June 2018

Rapid whole-genome mutational profiling using next-generation sequencing technologies

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PubMed Central

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31 October 2018

A general approach to the analysis of errors and failure modes in the base-calling function in automated fluorescent DNA sequencing.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709925

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31 October 2018

An improved algorithm for matching biological sequences.

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709925

retrieved

31 October 2018

Identifiers

DOI

10.1186/1471-2105-10-175

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

DBLP publication ID

journals/bmcbi/HomerMN09

1 reference

stated in

DBLP Dataset 2021-01-02

retrieved

28 January 2021

PMC publication ID

2709925

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

PubMed publication ID

19508732

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19508732

retrieved

27 July 2017

ResearchGate publication ID

26278310

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