The serial analysis of chromatin occupancy technique (SACO) promises to become a widely used method for the unbiased genome-wide experimental identification of loci bound by a transcription factor of interest. We describe the first web-based automatic tool, termed sequence tag analysis and reporting tool (START), for processing SACO data generated by experiments performed for the yeast, fruit fly, mouse, rat or human genomes. The program uses as input sequences of inserts from a SACO library from which it extracts all SACO tags, maps them to genomic locations and annotates them. START returns detailed information about these tags including the genes, the genomic elements and the miRNA precursors found in their vicinity, and makes use of the...
Next-generation sequencing is revolutionizing the identification of transcription factor binding sit...
<p>The transcriptional start and stop sites of candidate sRNAs were determined by circular RACE. The...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2002.Includes bibliographi...
Background Microarray and DNA-sequencing based technologies continue to produce enormous amounts of...
Signal Track Analytical Research Tool (START), is a parallel system for analyzing large-scale genomi...
Motivation: One of the most important features of genomic DNA are the protein-coding genes. While it...
Accurate identification of transcription start sites (TSSs) is an essential step in the analysis of ...
Background: Chromatin immunoprecipitation (ChIP) followed by high-throughput sequencing (ChIP-seq) o...
A minimally addressed area in Saccharomyces cerevisiae research is the mapping of transcription star...
Genome-wide association studies and re-sequencing projects are revealing an increasing number of dis...
Background Genome-wide repeat sequences, such as LINEs, SINEs and LTRs share a considerable part of ...
International audienceBACKGROUND: Recent genome wide transcription factor binding site or chromatin ...
BACKGROUND: Transcription initiation is a key component in the regulation of gene expression. mRNA 5...
To support transcriptional regulation studies, we have constructed DBTSS (DataBase of Transcriptiona...
Summary: Insertional mutagenesis is a powerful method for gene discovery. To identify the location o...
Next-generation sequencing is revolutionizing the identification of transcription factor binding sit...
<p>The transcriptional start and stop sites of candidate sRNAs were determined by circular RACE. The...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2002.Includes bibliographi...
Background Microarray and DNA-sequencing based technologies continue to produce enormous amounts of...
Signal Track Analytical Research Tool (START), is a parallel system for analyzing large-scale genomi...
Motivation: One of the most important features of genomic DNA are the protein-coding genes. While it...
Accurate identification of transcription start sites (TSSs) is an essential step in the analysis of ...
Background: Chromatin immunoprecipitation (ChIP) followed by high-throughput sequencing (ChIP-seq) o...
A minimally addressed area in Saccharomyces cerevisiae research is the mapping of transcription star...
Genome-wide association studies and re-sequencing projects are revealing an increasing number of dis...
Background Genome-wide repeat sequences, such as LINEs, SINEs and LTRs share a considerable part of ...
International audienceBACKGROUND: Recent genome wide transcription factor binding site or chromatin ...
BACKGROUND: Transcription initiation is a key component in the regulation of gene expression. mRNA 5...
To support transcriptional regulation studies, we have constructed DBTSS (DataBase of Transcriptiona...
Summary: Insertional mutagenesis is a powerful method for gene discovery. To identify the location o...
Next-generation sequencing is revolutionizing the identification of transcription factor binding sit...
<p>The transcriptional start and stop sites of candidate sRNAs were determined by circular RACE. The...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2002.Includes bibliographi...