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1.0k
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Comment:
Comment: What are the values shown on DESEQ2 heatmap legend?
20 months ago by
karl.stamm
4.1k
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1
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2.1k
views
Comment:
Comment: AF = 0.5 in chrX, VCF of a male
20 months ago by
karl.stamm
4.1k
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0
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631
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Comment:
Comment: Why am I getting same linear regression lines for 'x' on 'y' and 'y' on 'x'?
23 months ago by
karl.stamm
4.1k
1
vote
1
reply
752
views
Comment:
Comment: PCA does not show distinction in groups
2.1 years ago by
karl.stamm
4.1k
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0
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1.9k
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Comment:
Comment: Non biology & computer professional interested in bioinformatics
2.5 years ago by
karl.stamm
4.1k
0
votes
1
reply
879
views
Comment:
Comment: probability of two samples sharing a SNP by error
2.6 years ago by
karl.stamm
4.1k
0
votes
1
reply
2.0k
views
Comment:
Comment: SNP Pruning Through PCA
2.7 years ago by
karl.stamm
4.1k
1
vote
0
replies
722
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Comment:
Comment: Advise for a computational neophyte
2.7 years ago by
karl.stamm
4.1k
0
votes
0
replies
866
views
Comment:
C: On understanding the axis of a PCA plot
3.2 years ago by
karl.stamm
4.1k
0
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1
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1.3k
views
Comment:
C: [RNA-seq] Extremely Unconsistent Raw Count from Different Tools; a dark mistery
3.2 years ago by
karl.stamm
4.1k
0
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0
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2.5k
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Comment:
C: A question on the interpretation of a PCA plot
3.2 years ago by
karl.stamm
4.1k
0
votes
1
reply
935
views
Comment:
C: Very high ratio of cases to controls - how to increase statistical power?
3.2 years ago by
karl.stamm
4.1k
0
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1
reply
935
views
Comment:
C: Very high ratio of cases to controls - how to increase statistical power?
3.2 years ago by
karl.stamm
4.1k
0
votes
1
reply
808
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Comment:
C: Problems with the same gene names in R, any help?
3.2 years ago by
karl.stamm
4.1k
0
votes
0
replies
4.8k
views
Comment:
C: PEPATAC error: ConnectionResetError: [Errno 104] Connection reset by peer
3.3 years ago by
karl.stamm
4.1k
0
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0
replies
6.8k
views
Comment:
C: How to handle duplicate row names in R
3.3 years ago by
karl.stamm
4.1k
0
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0
replies
1.7k
views
Comment:
C: During RNA-seq analysis a lot of pseudogenes come up as DE
3.3 years ago by
karl.stamm
4.1k
1
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0
replies
3.8k
views
Comment:
C: What are the 5 biggest challenges/ opportunities in Bioinformatics going into 20
3.3 years ago by
karl.stamm
4.1k
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0
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2.4k
views
Comment:
C: Is there a tool to predict if a missense variant causes a loss of function on th
3.3 years ago by
karl.stamm
4.1k
0
votes
1
reply
2.5k
views
Comment:
C: A question on the interpretation of a PCA plot
3.4 years ago by
karl.stamm
4.1k
0
votes
0
replies
986
views
Comment:
C: Optimal Number of SNPs in NA12878 WES Data
3.4 years ago by
karl.stamm
4.1k
0
votes
1
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986
views
Comment:
C: Optimal Number of SNPs in NA12878 WES Data
3.4 years ago by
karl.stamm
4.1k
0
votes
1
reply
599
views
Comment:
C: Mapping transcriptomes against each other to find genetic differences
3.4 years ago by
karl.stamm
4.1k
0
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0
replies
1.4k
views
Comment:
C: Convert R script to python(implementation of the UPGMA OR neighbor joining algor
3.4 years ago by
karl.stamm
4.1k
0
votes
0
replies
1.2k
views
Comment:
C: Transforming big file
3.4 years ago by
karl.stamm
4.1k
0
votes
1
reply
1.2k
views
Comment:
C: Transforming big file
3.4 years ago by
karl.stamm
4.1k
1
vote
0
replies
875
views
Comment:
C: Wes analysis - Quality control on sequenced data
3.4 years ago by
karl.stamm
4.1k
0
votes
1
reply
711
views
Comment:
C: What is the smallest number of cases you can have in a GWAS before interpretatio
3.4 years ago by
karl.stamm
4.1k
0
votes
1
reply
4.4k
views
Comment:
C: how do I find the genes which are common to and those which differ between multi
3.5 years ago by
karl.stamm
4.1k
0
votes
0
replies
3.4k
views
Comment:
C: Why is gnomAD AF vs gnomAD exome AF so different?
3.5 years ago by
karl.stamm
4.1k
0
votes
0
replies
1.0k
views
Comment:
C: How to do a multi-snp/haplotype based GWAS instead of a single snp GWAS in R?
3.5 years ago by
karl.stamm
4.1k
0
votes
1
reply
1.9k
views
Comment:
C: Interpreting theta value
3.5 years ago by
karl.stamm
4.1k
0
votes
1
reply
1.0k
views
Comment:
C: How to do a multi-snp/haplotype based GWAS instead of a single snp GWAS in R?
3.5 years ago by
karl.stamm
4.1k
0
votes
0
replies
1.2k
views
Comment:
C: Publicly Available RNA-Seq Datasets from Human Heart
3.5 years ago by
karl.stamm
4.1k
0
votes
0
replies
1.0k
views
Comment:
C: Should we Ignore heterozygous SNPs while constructing SNP based phylogeny
3.5 years ago by
karl.stamm
4.1k
0
votes
1
reply
987
views
Comment:
C: Genes inhibiting each other's expression
3.6 years ago by
karl.stamm
4.1k
2
votes
0
replies
2.9k
views
Comment:
C: Why are we assuming most genes are not differentially expressed?
3.6 years ago by
karl.stamm
4.1k
1
vote
0
replies
1.1k
views
Comment:
C: Does 1000 genomes have a flat file with allele frequencies for each site anywher
3.6 years ago by
karl.stamm
4.1k
1
vote
0
replies
654
views
Comment:
C: Resources for learning how to submit jobs in unix-based cluster
3.6 years ago by
karl.stamm
4.1k
0
votes
1
reply
1.5k
views
Comment:
C: rnammer error :the command line on the script does not work
3.7 years ago by
karl.stamm
4.1k
0
votes
1
reply
1.5k
views
Comment:
C: rnammer error :the command line on the script does not work
3.7 years ago by
karl.stamm
4.1k
1
vote
1
reply
1.2k
views
Comment:
C: blastn much slower on longer subject sequences?
3.7 years ago by
karl.stamm
4.1k
1
vote
0
replies
1.7k
views
Comment:
C: For loop error for merging HTSeq counts
3.7 years ago by
karl.stamm
4.1k
0
votes
1
reply
1.2k
views
Comment:
C: blastn much slower on longer subject sequences?
3.7 years ago by
karl.stamm
4.1k
0
votes
0
replies
776
views
Comment:
C: Conserved regions around mutations
3.7 years ago by
karl.stamm
4.1k
1
vote
1
reply
776
views
Comment:
C: Conserved regions around mutations
3.7 years ago by
karl.stamm
4.1k
2
votes
1
reply
3.9k
views
Comment:
C: How do I process a FASTQ file in RStudio?
3.7 years ago by
karl.stamm
4.1k
0
votes
1
reply
2.5k
views
Comment:
C: How do I setup the pre-built indexed reference for Bowtie2
3.7 years ago by
karl.stamm
4.1k
0
votes
1
reply
18k
views
Comment:
C: Markduplicates: Value Was Put Into Pairinfomap More Than Once
3.8 years ago by
karl.stamm
4.1k
0
votes
0
replies
2.4k
views
Comment:
C: Does anyone know any ANNOVAR alternatives for Whole Genome Sequencing with flexi
3.8 years ago by
karl.stamm
4.1k
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