Strand-seq is a single-cell sequencing technique to finely map sister chromatid exchanges (SCEs) and other rearrangements. To analyze these data, we introduce BAIT, software which assigns templates and identifies and localizes SCEs. We demonstrate BAIT can refine completed reference assemblies, identifying approximately 21 Mb of incorrectly oriented fragments and placing over half (2.6 Mb) of the orphan fragments in mm10/GRCm38. BAIT also stratifies scaffold-stage assemblies, potentially accelerating the assembling and finishing of reference genomes. BAIT is available at http://sourceforge.net/projects/bait/.</p
Motivation: Strand-seq is a specialized single-cell DNA sequencing technique centered around the dir...
Genome editing has shown great promise for clinical translation but also revealed the risk of genoto...
De novo Genome assembly and k-mer frequency counting are two of the classical prob- lems of Bioinfo...
Strand-seq is a single-cell sequencing technique to finely map sister chromatid exchanges (SCEs) and...
Strand-seq is a single-cell sequencing technique to finely map sister chromatid exchanges (SCEs) and...
A Summary: Massively parallel sequencing is now widely used, but data interpretation is only as good...
Accurate reference genome sequences provide the foundation for modern molecular biology and genomics...
Homologous recombination involving sister chromatids is the most accurate, and thus most frequently ...
DNA rearrangements such as sister chromatid exchanges (SCEs) are sensitive indicators of genomic str...
Studies of genome heterogeneity and plasticity aim to resolve how genomic features underlie phenotyp...
Motivation: Strand-seq is a specialized single-cell DNA sequencing technique centered around the dir...
Genome editing has shown great promise for clinical translation but also revealed the risk of genoto...
De novo Genome assembly and k-mer frequency counting are two of the classical prob- lems of Bioinfo...
Strand-seq is a single-cell sequencing technique to finely map sister chromatid exchanges (SCEs) and...
Strand-seq is a single-cell sequencing technique to finely map sister chromatid exchanges (SCEs) and...
A Summary: Massively parallel sequencing is now widely used, but data interpretation is only as good...
Accurate reference genome sequences provide the foundation for modern molecular biology and genomics...
Homologous recombination involving sister chromatids is the most accurate, and thus most frequently ...
DNA rearrangements such as sister chromatid exchanges (SCEs) are sensitive indicators of genomic str...
Studies of genome heterogeneity and plasticity aim to resolve how genomic features underlie phenotyp...
Motivation: Strand-seq is a specialized single-cell DNA sequencing technique centered around the dir...
Genome editing has shown great promise for clinical translation but also revealed the risk of genoto...
De novo Genome assembly and k-mer frequency counting are two of the classical prob- lems of Bioinfo...