Nemo – A stochastic, individual-base, genetically explicit simulation platform
A recombination map has been added for all multi-locus traits. The map po...pic loci with several bi- or multi-allelic models. Spatial and temporal variation of selection on quantita...2784 days ago
2784 days ago
2165 days ago
Entrez Direct: E-utilities on the UNIX Command Line
Entrez Direct (EDirect) is an advanced method for accessing the NCBI's suite of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from a UNI...2766 days ago
2764 days ago
2751 days ago
2726 days ago
BIMA V3: an aligner customized for mate pair library sequencing
Summary: Mate pair library sequencing is an effective and economical method for detecting genomic structural variants and chromosomal abnormalities. Unfortunately, the...ed-end read contamination, chimeras, etc.), and presence of structura...2710 days ago
GenomeRing: alignment visualization based on SuperGenome coordinates
...allowing for comparative analyses of genomic variation. Such analyses are often based on whole-genome alignments to elucidate structural differences arising from ins...sive interpretation of all important genomic variations together with various supple...2675 days ago
2646 days ago