Assessing the impact of human genome annotation choice on RNA-seq expression estimates.
- Published in:
- BMC Bioinformatics, 2013, v. 14, n. Suppl 11, p. S8, doi. 10.1186/1471-2105-14-S11-S8
- By:
- Publication type:
- Article
Works matching IS 14712105 AND DT 2013 AND VI 14 AND IP Suppl 11
Results: 8
1
2
An efficient and scalable graph modeling approach for capturing information at different levels in next generation sequencing reads.
- Published in:
- BMC Bioinformatics, 2013, v. 14, n. Suppl 11, p. S7, doi. 10.1186/1471-2105-14-S11-S7
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- Publication type:
- Article
3
Provenance in bioinformatics workflows.
- Published in:
- BMC Bioinformatics, 2013, v. 14, n. Suppl 11, p. S6, doi. 10.1186/1471-2105-14-S11-S6
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- Publication type:
- Article
4
A base composition analysis of natural patterns for the preprocessing of metagenome sequences.
- Published in:
- BMC Bioinformatics, 2013, v. 14, n. Suppl 11, p. S5, doi. 10.1186/1471-2105-14-S11-S5
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- Publication type:
- Article
5
libgapmis: extending short-read alignments.
- Published in:
- BMC Bioinformatics, 2013, v. 14, n. Suppl 11, p. S4, doi. 10.1186/1471-2105-14-S11-S4
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- Publication type:
- Article
6
Efficient digest of high-throughput sequencing data in a reproducible report.
- Published in:
- BMC Bioinformatics, 2013, v. 14, n. Suppl 11, p. 1, doi. 10.1186/1471-2105-14-S11-S3
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- Publication type:
- Article
7
Fast discovery and visualization of conserved regions in DNA sequences using quasi-alignment.
- Published in:
- BMC Bioinformatics, 2013, v. 14, n. Suppl 11, p. 1, doi. 10.1186/1471-2105-14-S11-S2
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- Publication type:
- Article
8
Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives.
- Published in:
- BMC Bioinformatics, 2013, v. 14, n. Suppl 11, p. 1, doi. 10.1186/1471-2105-14-S11-S1
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- Publication type:
- Article