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of gains and losses of the motif sequence found at chromosome breakpoints using our collection of well-assembled genomes at different evolutionary scales (haplotypes, strains, and species) via bioinformatic
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treatment. It is advantageous if you have previously worked with massively parallel sequencing (NGS), both in the laboratory and/or with bioinformatics, for example Single Cell RNAseq. It is also advantageous
Searches related to parallel processing bioinformatics
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