![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
mitochondrial sequences | deepakpatilp | RNA Sequencing | 9 | 05-13-2015 10:01 AM |
repeating chipseq or chipseq with another antibody | hawainpanda | Sample Prep / Library Generation | 2 | 03-12-2015 04:56 PM |
Indexing ChIPseq libraries using Illumina's TruSeq and ChIPseq kits | Alex Clop | Epigenetics | 6 | 11-08-2012 12:07 PM |
known TF target genes in chipSeq dataset | honey | Bioinformatics | 2 | 04-10-2012 12:30 AM |
How do you identify the specific start and stop locations of mitochondrial genes | gwilymh | General | 1 | 03-10-2012 07:26 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Member
Location: australia Join Date: Jan 2011
Posts: 81
|
![]()
I have a dataset where chipseq was performed and I am looking specifically for mitochondrial genes. Is there a special work flow which I may use or normal BWa aligners should be used and follow the regular approach of calling peaks with MACS or SICER.
Thanks |
![]() |
![]() |
![]() |
#2 |
Member
Location: Australia Join Date: Aug 2010
Posts: 10
|
![]()
Use a standard ChIP-seq pipeline which includes binning the genome or peakfinding followed by differential expression with edgeR or DESeq then search through those results located on chrM or MT.
|
![]() |
![]() |
![]() |
Thread Tools | |
|
|