Found: 7
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iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data.
- Published in:
- BMC Systems Biology, 2013, v. 7, p. 1, doi. 10.1186/1752-0509-7-S6-S8
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- Publication type:
- Article
Human genetic research, race, ethnicity and the labeling of populations: recommendations based on an interdisciplinary workshop in Japan.
- Published in:
- BMC Medical Ethics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1472-6939-15-33
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- Publication type:
- Article
HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data.
- Published in:
- BMC Genomics, 2015, v. 16, p. 1, doi. 10.1186/1471-2164-16-S2-S7
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- Publication type:
- Article
TIGAR2: sensitive and accurate estimation of transcript isoform expression with longer RNA-Seq reads.
- Published in:
- BMC Genomics, 2014, v. 15, p. 1, doi. 10.1186/1471-2164-15-S10-S5
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- Publication type:
- Article
Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population.
- Published in:
- BMC Genomics, 2014, v. 15, n. 1, p. 673, doi. 10.1186/1471-2164-15-673
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- Publication type:
- Article
SUGAR: graphical user interface-based data refiner for high-throughput DNA sequencing.
- Published in:
- BMC Genomics, 2014, v. 15, n. 1, p. 664, doi. 10.1186/1471-2164-15-664
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- Publication type:
- Article
Estimating copy numbers of alleles from population-scale high-throughput sequencing data.
- Published in:
- BMC Bioinformatics, 2015, v. 16, p. S4, doi. 10.1186/1471-2105-16-S1-S4
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- Publication type:
- Article