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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...
De Novo Transcriptome Analysis (No Reference Based) ยท In this article, I will walk you through how to conduct a de novo transcriptome analysis. If you...
Good job! By now you should be able to download FASTA/FASTQ files with ease. The next series of write-ups will be about the high throughput sequence...