Hello... Can anyone tell me how to maintain the consistency of the initial or raw data downloaded from ncbi site... Like the bacterial genus i …

Hello, ***emphasized text***I need to analyse mtDNA sequencing data(sequence after multi-PCR which means no nuclear reads). I google and found mtDNA server, however this pipeline …

Hi, Can anyone tell me that how to filter primary alignment from the bam file. i have paired end data and mapped the data on …

Hello friends, i am new in this field, can anyone please help me in designing biological pathway. how to design biological pathways? what are the …

Hellow, I am using CLC for assembling genome. can anyone here please tell me how to find the percentage of genic and intergenic regions in …

Hello everyone, I have ion torrent short single-end reads and assembled data (CLC genomics workbench) of a plant. Can anyone tell me 1. I should …

Hey, I'm a beginner at Galaxy so I am currently going through their tutorials and exercises. Can any of you please explain how do I …

<p>can anyone please tell me the script to check the size of the each given contig (contigs are in multi-fasta format).</p>

Can anyone tell me what to do after getting a large no. of ORF of newly bacterial sequence which has not yet been submitted to …

<p>hello everyone.</p> <p>can anyone tell me how can i do multiple sequence blast with tigr transcript assembly database...... i need to analyse the blast result …