User: luckysardar171
luckysardar171 • 0
- Reputation:
- 0
- Status:
- New User
- Last seen:
- 15 hours ago
- Joined:
- 5 months, 2 weeks ago
- Email:
- l*************@gmail.com
Profile information, website and location are not shown for new users.
This helps us discourage the inappropriate use of our site.
Posts by luckysardar171
<prev
• 31 results •
page 1 of 4 •
next >
0
votes
0
answers
58
views
0
answers
... Any suggestions will be helpful
Thank you
...
written 1 day ago by
luckysardar171 • 0
0
votes
0
answers
58
views
0
answers
... Hello I am doing chip experiment is IgG is needed in the experiments or Input DNA enough, experience people suggestions will be very helpful, I went through many biostar threads people are suggesting Input DNA as a control will be enough, and from some literature survey I understand that some spuri ...
written 2 days ago by
luckysardar171 • 0
0
votes
1
answer
49
views
1
answers
... Okay Thank you. for my experiment I have one wt and knockout data i wanted compare this two and show the H3K4me3 status how I have to proceed, do the differential analysis or what, any examples and papers will be better to understand
Thank you ...
written 3 days ago by
luckysardar171 • 0
0
votes
1
answer
49
views
1
answers
... Okay Thank you for your suggestions, can you please tell me usage of --SPMR in MACS2 because encode project uses in its pipeline ...
written 3 days ago by
luckysardar171 • 0
2
votes
1
answer
49
views
1
answer
... Hello currently I am working on Chip-seq analysis i have paired end data 35-130 PE reads I have aligned with bowtie2, after mapping generated the bam. Using MACS2 i wanted call the peaks(H3K4me3 histone mark) when I run run_spp.R for Modelling Fragment Size i got the below output result i am little ...
written 3 days ago by
luckysardar171 • 0
0
votes
0
answers
64
views
0
answers
... Okay, thank you for the reply, My fragment size varying lot does it matters in chip-seq ...
written 6 days ago by
luckysardar171 • 0
0
votes
0
answers
64
views
0
answers
... Hello everyone I am analyzing Chip-seq data. In fragmentation step we used Micrococcal Nuclease in this condition can I remove duplicate reads from bam file after mapping or not can anyone suggest me. Read many related papers some people are removing duplicates and some are not confused what to do. ...
written 6 days ago by
luckysardar171 • 0
0
votes
1
answer
131
views
1
answers
... Peak number mentioned is over Input, is there any necessary to make all sample with same library size. ...
written 17 days ago by
luckysardar171 • 0
0
votes
1
answer
131
views
1
answers
...
The below plot I got it from plotfingerprint can you please give some comments
https://ibb.co/FBHJzn3 ...
written 18 days ago by
luckysardar171 • 0
0
votes
1
answer
131
views
1
answers
... Okay, Thank you...so much ...
written 18 days ago by
luckysardar171 • 0
Latest awards to luckysardar171
No awards yet. Soon to come :-)
Use of this site constitutes acceptance of our User
Agreement
and Privacy
Policy.
Powered by Biostar
version 2.3.0
Traffic: 1505 users visited in the last hour