웹2024년 1월 29일 · This tool calculates the fragment sizes for read pairs given a BAM file from paired-end sequencing.Several regions are sampled depending on the size of the genome and number of processors to estimate thesummary statistics on the fragment lengths. Properly paired reads are preferred for computation, i.e., it will only use discordant pairs if no ... 웹2024년 9월 16일 · Peak Calling. Peak calling, the next step in our workflow, is a computational method used to identify areas in the genome that have been enriched with aligned reads as a consequence of performing a ChIP-sequencing experiment. For ChIP-seq experiments, what we observe from the alignment files is a strand asymmetry with read densities on the ...
Learning the BAM format - GitHub Pages
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ATAC-seq data analysis: from FASTQ to peaks - Yiwei Niu
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