Hello everyone, I am using Haploview to find the tag SNPs in my data. while preparing the input file, the format ask for .info file …

We are looking into the possibility of off-target mapping for some sequences that were added to our alignment reference. We are only concerned about off-target …

How many samples can we pooled for Bacterial RNA seq in Miseq system and what will be ideal reads

Hello, I a newbie in bioinformatics. I am now analyzing whole exome sequencing data, and the samples are normal tumor matched. I am currently using …

Hi friends, Recently, we performed exome sequencing for 3 samples using Nextera sequencing machine. We used new kit for exome sequencing. So I am interested …

I have a pooled RNA seq data from 5 to 10 individuals at different stages. I want to assemble them and combine all of data …

Hi people, I am trying to assemble pacbio reads from RS II. But, the problem is that 1) we have pooled 6 BAC clones per …

Hi, We have identified SNPs in biological replicates (x3) for each population (in vcf files) from RNA-Seq data. My question is: how do we calculate …

<p>Which is better foe pooled data?GATK variant call or Syzygy variant call?</p>

<p>Which is better to use? Annovar or Syzygy?? What is the difference between both ?</p>