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Variant Calling is used when one wants to identify differences in genomic sequence such as SNP (single nucleotide polymorphism), insertions, deletions...
Reference Based Transcriptome Analysis (Genome Mapping) · Preliminary Preparation: Before we start, there are a couple of tools (hyperlinked) to...
Using Trimmomatic to Clean High Throughput Sequence Data · Now that you have assessed the quality of your sequenced data using FastQC, it's time to...
How to Process Files in Bulk through FastQC: Linux Commands, Bash script, and MultiQC · There are several ways to process multiple FASTQ files through...
