Latest
Open
RNA-Seq
ChIP-Seq
SNP
Assembly
Tutorials
Tools
Jobs
Forum
Planet
All »
Home
Log In

User: spacemorrissey

gravatar for spacemorrissey
Reputation:
210
Status:
Trusted
Location:
United States
Website:
https://scholar.google...
Last seen:
1 month ago
Joined:
6 years, 1 month ago
Email:
s*************@gmail.com

about me

Posts by spacemorrissey

<prev • 35 results • page 1 of 4 • next >
1
vote
1
answer
622
views
1
answers
Answer: A: What is the reasonable proportion of zero counts in single-cell RNA-Seq data
... Unfortunately the answer to this would be very organism and cell type specific. It would also depend on the depth of sequencing that you performed. From normal RNA-seq from a population of cells there are often 1/3 to 1/2 of genes that are not expressed at levels above noise. I would think that i ...
written 10 months ago by spacemorrissey • 210
1
vote
2
answers
1.5k
views
2
answers
Answer: A: What is the "sliding window" in a bio statistical analysis, e.g. in a genome seq
... Very simply, you take a window of some size, 10, 100, 1000 base pairs. You can then answer some question about what happens in that window. How many mutation occur in this window, how many reads align to this window, etc. The you slide the window by moving the window by some number of basepaires. ...
written 10 months ago by spacemorrissey • 210
3
votes
2
answers
1.2k
views
2
answers
Answer: A: How can I look at find 'open chromatin' from ATAC-seq data using MACS2
... You can use MACS, but it is not the best tool for identifying open chromatin regions. I would recommend using Fseq: http://fureylab.web.unc.edu/software/fseq/ It was designed to analyze DNase -seq data, the predecessor of ATAC-seq. When analyzing data from either experiment, you do not really wa ...
written 10 months ago by spacemorrissey • 210
0
votes
0
answers
297
views
0
answers
Comment: C: Analyzing CRISPR and RNAi genome wide screens
... I found this paper "Systematic comparison of CRISPR-Cas9 and RNAi screens for essential genes" https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4900911/ Has anyone used this? Has anyone found anything better? ...
written 10 months ago by spacemorrissey • 210
0
votes
0
answers
297
views
0
answers
Analyzing CRISPR and RNAi genome wide screens
... I have data from genome wide CRISPR and RNAi gene knockdown screens. These were pooled experiments where genes were either knocked out with CRISPR or knocked down with RNAi, and then the surviving cells were sequenced. Tags corresponding to lethal knockouts would therefore be depleted in the resul ...
crispr meta analysis rnai written 10 months ago by spacemorrissey • 210
1
vote
1
answer
462
views
1
answer
Metabolomics Analysis - missing value imputation
... Hello, I am looking for some guidance on metabolomics analysis. I have a data set that has missing values for many of the metabolites, and I am wondering what the best method for dealing with that is. If I limit myself to metabolites with no missing values I drop a huge amount of my data, but ...
metabolomics written 12 months ago by spacemorrissey • 210 • updated 12 months ago by Kevin Blighe ♦ 42k
0
votes
1
answer
460
views
1
answers
Comment: C: how many columns does F-seq need in the bed file
... Oops the text editor wrapped the lines of data. Just give it: Chrom start stop . . strand ...
written 22 months ago by spacemorrissey • 210
0
votes
1
answer
460
views
1
answers
Answer: A: how many columns does F-seq need in the bed file
... All F-seq really needs is the chrome, start position, and strand, but it expects to find that in bed format. So you should send it a file with 6 columns as below. Columns 4 and 5 are ignored, so you can put what ever you want in there. Also, since F-seq works on the density of cut sites, not an o ...
written 22 months ago by spacemorrissey • 210
0
votes
1
answer
1.4k
views
1
answers
Comment: C: How to report differentially expressed transcription factors in scatter plot
... plotting FPKM in men vs women should give you what you wanted. I do not think you want to be plotting the FDR values. ...
written 2.5 years ago by spacemorrissey • 210
1
vote
1
answer
1.4k
views
1
answers
Answer: A: How to report differentially expressed transcription factors in scatter plot
... Assuming that your replicates look good, you can definitely plot the mean on replicates in one condition against the mean of replicates in the other condition. You can then highlight and annotate the differentially expressed genes on the plot. Another common way to display this type of analysis is ...
written 2.5 years ago by spacemorrissey • 210

Latest awards to spacemorrissey

Scholar 10 months ago, created an answer that has been accepted. For A: How can I look at find 'open chromatin' from ATAC-seq data using MACS2
Popular Question 22 months ago, created a question with more than 1,000 views. For What Is The Best Software For Finding Footprints In Mouse Dnase-Seq Data?
Popular Question 2.9 years ago, created a question with more than 1,000 views. For What Is The Best Software For Finding Footprints In Mouse Dnase-Seq Data?
Popular Question 4.3 years ago, created a question with more than 1,000 views. For What Is The Best Software For Finding Footprints In Mouse Dnase-Seq Data?
Teacher 5.1 years ago, created an answer with at least 3 up-votes. For A: I'M Looking For A Bioinformatics Problem Which Could Benefit From A New Or Impro
Content
Help
Access
Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1082 users visited in the last hour