73 search results - page 3 / 15 » Inference of Isoforms from Short Sequence Reads |
BMCBI
2010
14 years 10 months ago
2010
Background: We propose a method for deriving enzymatic signatures from short read metagenomic data of unknown species. The short read data are converted to six pseudo-peptide cand...
BICOB
2009
Springer
15 years 4 months ago
2009
Springer
The de novo assembly of genomes from high-throughput short reads is an active area of research. Several promising methods have been recently developed, with applicability mainly re...
RECOMB
2008
Springer
15 years 10 months ago
2008
Springer
Next Generation Sequencing (NGS) technologies are capable of reading millions of short DNA sequences both quickly and cheaply. While these technologies are already being used for r...
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BIBM
2010
IEEE
14 years 7 months ago
2010
IEEE
Advances in sequencing technologies have equipped researchers with the ability to sequence the collective genome of entire microbial communities commonly referred to as metagenomi...
BMCBI
2010
14 years 10 months ago
2010
Background: Polymorphic variants and mutations disrupting canonical splicing isoforms are among the leading causes of human hereditary disorders. While there is a substantial evid...