Accurate taxonomic assignment of short pyrosequencing reads. (1/2909)

Ambiguities in the taxonomy dependent assignment of pyrosequencing reads are usually resolved by mapping each read to the lowest common ancestor in a reference taxonomy of all those sequences that match the read. This conservative approach has the drawback of mapping a read to a possibly large clade that may also contain many sequences not matching the read. A more accurate taxonomic assignment of short reads can be made by mapping each read to the node in the reference taxonomy that provides the best precision and recall. We show that given a suffix array for the sequences in the reference taxonomy, a short read can be mapped to the node of the reference taxonomy with the best combined value of precision and recall in time linear in the size of the taxonomy subtree rooted at the lowest common ancestor of the matching sequences. An accurate taxonomic assignment of short reads can thus be made with about the same efficiency as when mapping each read to the lowest common ancestor of all matching sequences in a reference taxonomy. We demonstrate the effectiveness of our approach on several metagenomic datasets of marine and gut microbiota.  (+info)

Identification and classification of small RNAs in transcriptome sequence data. (2/2909)

Current methods for high throughput sequencing (HTS) for the first time offer the opportunity to investigate the entire transcriptome in an essentially unbiased way. In many species, small non-coding RNAs with specific secondary structures constitute a significant part of the transcriptome. Some of these RNA classes, in particular microRNAs and snoRNAs, undergo maturation processes that lead to the production of shorter RNAs. After mapping the sequences to the reference genome specific patterns of short reads can be observed. These read patterns seem to reflect the processing and thus are specific for the RNA transcripts of which they are derived from. We explore here the potential of short read sequence data in the classification and identification of non-coding RNAs.  (+info)

Targeted high-throughput DNA sequencing for gene discovery in retinitis pigmentosa. (3/2909)

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AutoMeDIP-seq: a high-throughput, whole genome, DNA methylation assay. (4/2909)

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Introduction into the analysis of high-throughput-sequencing based epigenome data. (5/2909)

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The next generation of molecular markers from massively parallel sequencing of pooled DNA samples. (6/2909)

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Next-generation genomics: an integrative approach. (7/2909)

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Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample. (8/2909)

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