Topic: sequencing-coverage Goto Github
Some thing interesting about sequencing-coverage
Some thing interesting about sequencing-coverage
sequencing-coverage,Analyze Whole Genome Bi-Sulfite Sequencing for Grape evolution in response to grafting
User: aryan092
sequencing-coverage,
Organization: broadinstitute
sequencing-coverage,Detection and correction of sequencing errors in protein coding regions of whole genome draft sequences
User: johannes-zi
sequencing-coverage,This is a pipeline for analyzing next-generation sequencing results. An aligned sequence in a BAM file is compared to a reference fasta file in order to assess depth of coverage as well as assist in determining single nucleotide variants and calculating Shannon entropy of the genome.
User: rastshawn
sequencing-coverage,Calculate fastq reads and sequencing coverage
User: raymondkiu
sequencing-coverage,a long read repeat coverage calculator,given an long read file before assembly either direct from the sequencing runs or after the cleaning, it calculates the total amount of the repeat stretches present in the sequencing reads and you can plot them before assembly
User: sablokgaurav
sequencing-coverage,Callable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer
User: sigven
sequencing-coverage,Software for predicting library complexity and genome coverage in high-throughput sequencing.
Organization: smithlabcode
Home Page: https://preseq.readthedocs.io
sequencing-coverage,An R package for estimating library complexity
Organization: smithlabcode
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