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Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...Sciences announced the latest version release of its bioinformatics flagship product, Strand NGS, at the Annual Meeting of the American Society of Human Genetics today. Two major the...2385 days ago
SeqMule: Automated human exome/genome variants detection
SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by l...2615 days ago
CABOG: Celera Assembler with Best Overlap Graph
...veloped at Celera for the 2001 publication of the first draft human genome sequence. The software...er, 2000). It was the first to assemble both parental haplotypes of one human genome (J. Craig Venter, 2007...2546 days ago
CAR: Reconstructing Contiguous Regions of an Ancestral Genome
...enome that accounts for 96.8% of the available human genome sequence data. The pre...the predicted evolutionary breakpoints in the human lineage confirms certain publ...ct the genome sequence of the last ancestor of human, dogs, and most other placent...2543 days ago
AVID: A Global Alignment Program
...ent numerous applications of the method, ranging from the comparison of assemblies to alignment of large syntenic genomic regions and whole genome human/mouse alignments. We have als...2537 days ago
Computational Genomics: Applied Comparative Genomics
...computational and quantitative approaches for comparing and analyzing genomes starting from raw sequencing data. The course will focus on human genomics and human medical applications, but the...2348 days ago