my sequences have names of more than 10 characters. but looks like phylip format takes only names with characters less than 10. How to deal …

Hi. I am a doctoral student. The binding structure is predicted using specific protein and peptide sequences. By the way, each time I do, I …

I want to find out if it is possible to filter the size of structural variants using the -x options. In the Pindel documentation -x …

If I sequence a tissue/blood sample from the same subject (human), how will the outputs from Illumina's Genome analyzer, Roche 454's Genome Sequencer, and Applied …

Hi guys~ I have two sets of proteins: let's say A set (contains 100 A genes) and B Set containing (100 B genes). I want …

Hi, Last time I mapped my data with STAR that took me less than two minutes. But this time for 0.1 percent of data it …

Hi! I have a protein sequence which is way more than 1000 aa residues. However, it does not have a crystal structure. So I obtained …

<p>Dear All,</p> <p>I want to analyse the microarray data using ARACNE graphic user interface. I follow the tutorial according to the paper published in nature …

<p>Obviously BLAST is going to have better on-average performance on a smaller database than on a larger database. But for a particular (large) database (let's …

<p>I hope I phrase this properly so it makes sense... I'm trying to provide annotations for indels and splice sites based on the HGVS standard …