You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
{{ message }}
This repository has been archived by the owner on Nov 8, 2021. It is now read-only.
Status:
I have the number of transposon and reads mapped per gene , but I do not have still the fastq files to our analysis using the pipeline.
Library: Each library is about 350.000 mapped insertions, which is great.
Explanation from Agnes about the technical replicates: A word about where "a" and "b" are coming from: when I split the ligation mix, I simply transferred half of the ligation into a fresh tube, and as usual added the PCR mix to the ligation. The reaction from the original tube was labeled "a"
The reaction from the fresh tube was labeled "b". "a" and "b" were barcoded with different indexes.
Particularities of my WT with respect Agnes WT For ex SPR6, SUT1, GEF1, etc In many of those cases , it seems that those genes are essential in your WT but not in mine
leilaicruz
changed the title
SATAY Data analysis from yll3a and dnrp1 strains
SATAY Data sequencing of WT and dnrp1 strains thanks to Agnes Michel (from Benoit lab, Oxford)
Feb 17, 2021
No description provided.
The text was updated successfully, but these errors were encountered: