Hi, I have the variant calling output in the form of `vcf` files. Variant calling was done with `GATK haplotypecaller`. I am interested in performing …
Hello, Let's say I have two or more complete bacterial genome sequences produced by Sanger sequencing and/or Nanopore/PacBio (no Illumina reads). The bacterial genomes in …
<p>I had sequenced 2 bacterial genomes using Illumina platform. The genomes were assembled and annotated which allows me to view the genetic distribution of the …
<p>Hi!</p> <p>I have three RNA-seq samples and by pairwise comparison I have computed differentially expressed genes between them.</p> <p>I have two questions:</p> <p>(i) Is there …