(Q40485973)

20 September 2017

title

SAMSVM: A tool for misalignment filtration of SAM-format sequences with support vector machine (English)

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20 September 2017

main subject

support vector machine

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5

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20 September 2017

Jianfeng Yang

1

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20 September 2017

Xiaofan Ding

series ordinal

2

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20 September 2017

Xing Sun

series ordinal

3

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20 September 2017

Shui-Ying Tsang

series ordinal

4

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20 September 2017

language of work or name

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24 August 2015

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Journal of Bioinformatics and Computational Biology

20 September 2017

published in

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20 September 2017

volume

13

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20 September 2017

issue

6

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20 September 2017

page(s)

1550025

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describes a project that uses

20 September 2017

support vector machine

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based on heuristic

inferred from title

cites work

The Sequence Alignment/Map format and SAMtools

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Sequencing technologies - the next generation

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Next-generation DNA sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

SOAP2: an improved ultrafast tool for short read alignment

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

SOAP3: ultra-fast GPU-based parallel alignment tool for short reads

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Fast gapped-read alignment with Bowtie 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Fast and accurate short read alignment with Burrows-Wheeler transform

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Benchmarking short sequence mapping tools

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Uncertainty in homology inferences: assessing and improving genomic sequence alignment

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

PCR amplification introduces errors into mononucleotide and dinucleotide repeat sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Targeted high throughput sequencing of a cancer-related exome subset by specific sequence capture with a fully automated microarray platform

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

A framework for variation discovery and genotyping using next-generation DNA sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Classification of multiple cancer types by multicategory support vector machines using gene expression data

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Splice site identification using probabilistic parameters and SVM classification.

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

A support vector machine for identification of single-nucleotide polymorphisms from next-generation sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

AluScan: a method for genome-wide scanning of sequence and structure variations in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Accurate estimation of short read mapping quality for next-generation genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

An integrated semiconductor device enabling non-optical genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

Microsatellite marker discovery using single molecule real-time circular consensus sequencing on the Pacific Biosciences RS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1142%2FS0219720015500250

10.1142/S0219720015500250

21 January 2018

Identifiers

DOI

1 reference

20 September 2017

DBLP publication ID

journals/jbcb/YangDSTX15

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference