User: morovatunc

gravatar for morovatunc
morovatunc400
Reputation:
400
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Trusted
Location:
Turkey
Twitter:
mortunco
Last seen:
1 day, 22 hours ago
Joined:
4 years, 4 months ago
Email:
m*********@gmail.com

Posts by morovatunc

<prev • 193 results • page 1 of 20 • next >
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Comment: C: How to calculate dinucleotide A/T patterns in a given human reference genome reg
... consensusMatrix(dinucleotideFrequency(DNA.set)) ? maybe ? ...
written 10 months ago by morovatunc400
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Comment: C: How to calculate dinucleotide A/T patterns in a given human reference genome reg
... dinucleotideFrequency function of biostrings could give those 2mers. than you can take the subset of your desired ones. ...
written 10 months ago by morovatunc400
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Comment: C: Finding Chip Seq Overlaps with Bed files
... "based on my experience" ...
written 10 months ago by morovatunc400
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Answer: A: Finding Chip Seq Overlaps with Bed files
... For the ones who has not found an answer. Homer's mergePeak function exactly what I want. Link itself is pretty explanatory. http://homer.ucsd.edu/homer/ngs/mergePeaks.html However, author seems not to respond problems related with the software so heads up. ...
written 10 months ago by morovatunc400
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Answer: A: IGV/IGB add two lines in a track
... Hi. For bigwigs, I think you can use IGV's Overlay Tracks function. So select your tracks, right click and choose Overlay Tracks from right click menu. These are the screen shots. https://ibb.co/nQsmWL https://ibb.co/kUB25f Hope this helps, Tunc. ...
written 13 months ago by morovatunc400
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Comment: C: FIMO output that preserves padj values
... I think your method is much better. ...
written 14 months ago by morovatunc400
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Comment: C: FIMO output that preserves padj values
... I dont have your data at the moment therefore I cannot give explicit solution but I can show you the way R has a function called merge.data.frame. We are gonna use this to merge your initial data with the latest fimo output. So In the end you will have BED + fimo merged together. (probably, you wil ...
written 14 months ago by morovatunc400
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Amplicon based sequencing Mutation Calling
... Dear all, We are investigating the effect of TF-mediated mutations on genome. In the validation part, we narrowed our regions to 1. We sequenced this region and upstream of it and obtained ~100 k coverage with paired end reads. This is our experimental setup. So we simple want to compare mutation f ...
sequence mutation calling sequencing written 14 months ago by morovatunc400
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Comment: C: Does anybody success to download data using icgc-storage-client ?
... I think you should write to ICGC help desk. They are very helpful. Also I suggest you to log in to the spesific ec2 region. As far as I know, USA ec2 servers have access to icgc data. Final thing, make sure you set your key code. (The code that lets you access to the restricted data.) ...
written 18 months ago by morovatunc400
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Comment: C: Starrseq data how can I characterise reads that maps out of the targeted regions
... Yeah. I think it is cap-starrseq because I remember the preparation of the array design, forward and reverse primers etc. (Sorry for my ignorance, I mainly focus on the computational part of this project.) Could you help me to understand why you are not very concerned with %70 unspecific mappings?( ...
written 18 months ago by morovatunc400

Latest awards to morovatunc

Popular Question 6 months ago, created a question with more than 1,000 views. For VCF filtration problem No genotype information
Popular Question 6 months ago, created a question with more than 1,000 views. For Variant Calling output problem GL000 contigs
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Popular Question 6 months ago, created a question with more than 1,000 views. For About Dream Challenge Somatic Mutation Calling Algorithms
Popular Question 6 months ago, created a question with more than 1,000 views. For HOMER mergePeaks -d value definition
Popular Question 7 months ago, created a question with more than 1,000 views. For VCF filtration problem No genotype information
Popular Question 7 months ago, created a question with more than 1,000 views. For Variant Calling output problem GL000 contigs
Popular Question 7 months ago, created a question with more than 1,000 views. For VarDictJava BED file input Problem
Popular Question 8 months ago, created a question with more than 1,000 views. For VCF filtration problem No genotype information
Popular Question 8 months ago, created a question with more than 1,000 views. For VCF filtration problem No genotype information
Popular Question 9 months ago, created a question with more than 1,000 views. For VCF filtration problem No genotype information
Popular Question 10 months ago, created a question with more than 1,000 views. For VCF filtration problem No genotype information
Popular Question 10 months ago, created a question with more than 1,000 views. For Finding Chip Seq Overlaps with Bed files
Popular Question 10 months ago, created a question with more than 1,000 views. For Finding Chip Seq Overlaps with Bed files
Popular Question 12 months ago, created a question with more than 1,000 views. For Finding Chip Seq Overlaps with Bed files
Popular Question 13 months ago, created a question with more than 1,000 views. For CRISPR screen Trimming with mageck low mappability
Popular Question 14 months ago, created a question with more than 1,000 views. For CRISPR screen Trimming with mageck low mappability
Popular Question 14 months ago, created a question with more than 1,000 views. For Finding Chip Seq Overlaps with Bed files
Great Question 17 months ago, created a question with more than 5,000 views. For Kallisto New RNA-seq quantification method discussion
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Popular Question 17 months ago, created a question with more than 1,000 views. For Finding Chip Seq Overlaps with Bed files

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