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Forum: Bioinformatics 07-19-2018, 11:08 AM
Replies: 2
Views: 1,067
Posted By seqance
Thank you GenoMAx

Thank you GenoMAx
Forum: Bioinformatics 07-19-2018, 10:50 AM
Replies: 2
Views: 1,067
Posted By seqance
Reads color in IGV

Hi everyone,
What's the difference between red, blue and grey reads in IGV?
Many thanks
Forum: General 07-16-2018, 02:21 AM
Replies: 0
Views: 1,602
Posted By seqance
NGS informations

Hi,
I'am not very familiar with NGS and have a lot of (naive) questions e.g:
How to determine size of library using Bioanalyzer?
Bioanalyzer provide me a table with several sizes (pb) with...
Forum: Introductions 06-22-2018, 01:39 PM
Replies: 1
Views: 2,693
Posted By seqance
NGS Exome sequencing

Hello,
how can i calculate the depth and the coverage if sequencing exome panel using Miseq?
thank you a lot.
Forum: General 06-01-2018, 04:55 AM
Replies: 6
Views: 2,148
Posted By seqance
Thank you ECO. would you suggest me 'websites or...

Thank you ECO. would you suggest me 'websites or other ' to learn about nsg?
Forum: General 05-31-2018, 05:08 AM
Replies: 6
Views: 2,148
Posted By seqance
I'll try it next week. Thank you AT/GC.

I'll try it next week. Thank you AT/GC.
Forum: General 05-31-2018, 01:10 AM
Replies: 6
Views: 2,148
Posted By seqance
Hi AT/CG, Thank you for your reply. It is my...

Hi AT/CG,
Thank you for your reply.
It is my first library prep, beads were over dried because i saw cracks.
I ll try again and let beads dry for less time.
Forum: General 05-30-2018, 01:53 AM
Replies: 6
Views: 2,148
Posted By seqance
DNA bead purification

Hi all,
I am new in NGS library prep,when i purified DNA with beads i lost most of my input.
How to perform DNA purification using bead whithout losing material?
Could someone help?
Many thanks
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