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User: bioinfo89

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bioinfo89 • 40
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6 days, 17 hours ago
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2 years, 9 months ago
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k****************@yahoo.com

Posts by bioinfo89

<prev • 67 results • page 1 of 7 • next >
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ChIA-PET2: Error: Don't have enough confident interactions to learn the model.
... Hi All, I am currently getting the following error when I use ChIA-PET2: Running MICC... Intra data: ChIAPET_rawdata/rep1_ChIAPET.interactions.intra.bedpe Inter data: ChIAPET_rawdata/rep1_ChIAPET.interactions.inter.bedpe Output file: ChIAPET_rawdata/rep1_ChIAPET.interactions.M ...
chip-seq written 10 days ago by bioinfo89 • 40 • updated 9 days ago by RamRS ♦ 26k
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Comment: C: bedtools complement error
... Hi @Alex Reynolds, I was just exploring the bedpos `--complement` option instead of bedtools complement option to get coordinates which are present in `genome.bed` but not in `target.bed`, I found `--difference` is more suitable to get the `result.bed`, instead of `--complement`. Do correct me if ...
written 9 months ago by bioinfo89 • 40 • updated 9 months ago by RamRS ♦ 26k
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Comment: C: Where to get homopolymer annotation for human genome ?
... Hi @ATpoint, Thank you very much for the Rscript, I used it for extracting the homopolymers from reference genome. I wanted to know if there is a way to use the same script to limit the homopolymers finding in the coding regions only? ...
written 10 months ago by bioinfo89 • 40
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Comment: A: Where to get homopolymer annotation for human genome ?
... Hi @ATpoint, I would really appreciate if you could share the Rscript again. I couldn't find your Rscript. Thanks! ...
written 10 months ago by bioinfo89 • 40
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How to consider/get the g. positions for variants in introns?
... Hello All, My query is regarding the genomic positions to be considered for a variant which are present in the intron. For example: c.5278-1G>C, so the genomic position for c.5278 is 41203134. Since the above nomenclature is 5278-1 which will be 5277th position and is the last base of the intr ...
snp written 12 months ago by bioinfo89 • 40 • updated 12 months ago by finswimmer ♦ 13k
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Comment: C: Merge vcf files with multiple samples into one vcf with all variants
... Yes, I am trying my best. :) ...
written 16 months ago by bioinfo89 • 40
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Comment: C: Merge vcf files with multiple samples into one vcf with all variants
... By non-standard vcf I mean, it is a dbSNP submission VCF format which has additional information about the study and methods etc along with the reference assembly ID, INFO and FORMAT fields. Also, the INFO and FORMAT fields I had to remove since the tabidx step was not able to parse the information. ...
written 16 months ago by bioinfo89 • 40 • updated 16 months ago by WouterDeCoster ♦ 43k
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Comment: C: Merge vcf files with multiple samples into one vcf with all variants
... Yes sure I will test the vcflib tool kit thanks for the info. I used the following commands for vcftools: /home/tools/tabix-0.2.6/bgzip Validated.vcf /home/tools/tabix-0.2.6/tabix -p vcf Validated.vcf.gz /home/tools/vcftools_0.1.13/perl/vcf-compare Validated1.vcf.gz Validated2.vcf ...
written 16 months ago by bioinfo89 • 40 • updated 16 months ago by WouterDeCoster ♦ 43k
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Comment: C: How to merge multiple VCF files (each has multiple samples genotype) from differ
... I tried it. But since the file I am using is not a standard VCF file, I am not getting the desired output. The vcf-validator throws lots of errors when I check the files I am using. ...
written 16 months ago by bioinfo89 • 40
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Merge vcf files with multiple samples into one vcf with all variants
... Hi All, I am working on 1000g data. So I have 25 tab-delimited text files corresponding to each population. Each file has jointly genotyped data, so it contains genotypes from all the samples (~60-120) per population in the VCF. Format of the File: #CHROM POS ID REF ALT QUAL FILTER INFO FORMA ...
vcf snp written 16 months ago by bioinfo89 • 40 • updated 12 months ago by zx8754 ♦ 9.1k

Latest awards to bioinfo89

Great Question 5 months ago, created a question with more than 5,000 views. For Merge vcf files with multiple samples into one vcf with all variants
Popular Question 5 months ago, created a question with more than 1,000 views. For Primer3 error:./primer3_core: Input line with no '=':
Popular Question 12 months ago, created a question with more than 1,000 views. For Merge vcf files with multiple samples into one vcf with all variants
Popular Question 12 months ago, created a question with more than 1,000 views. For Primer3 error:./primer3_core: Input line with no '=':
Popular Question 14 months ago, created a question with more than 1,000 views. For Primer3 error:./primer3_core: Input line with no '=':
Supporter 16 months ago, voted at least 25 times.
Scholar 23 months ago, created an answer that has been accepted. For A: How to extract unique paired end reads from a merged BAM file?
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