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Comment:
Comment: bam-readcount compilation error
3.5 years ago by
Ram
45k
3
votes
1
reply
1.8k
views
Comment:
Comment: Unable to open pdf file of volcano plots created using many group comparisons fr
3.5 years ago by
Ram
45k
0
votes
0
replies
1.1k
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Comment:
Comment: How to merge VCF from disjoint sample lists
3.5 years ago by
Ram
45k
3
votes
1
reply
1.1k
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Answer:
Answer: How to merge VCF from disjoint sample lists
3.5 years ago by
Ram
45k
0
votes
1
reply
1.3k
views
Comment:
Comment: genome status
3.5 years ago by
Ram
45k
0
votes
0
replies
1.2k
views
Comment:
Comment: Heatmap rownames as gene names displayed as ensembl ID
3.5 years ago by
Ram
45k
0
votes
0
replies
959
views
Comment:
Comment: Clustering of samples based on gene expression
3.5 years ago by
Ram
45k
0
votes
0
replies
1.7k
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Comment:
Comment: Ensembl IDs
3.5 years ago by
Ram
45k
0
votes
0
replies
7.3k
views
Comment:
Comment: Csv. To VCF. File convert
3.5 years ago by
Ram
45k
0
votes
0
replies
1.3k
views
Comment:
Comment: genome status
3.5 years ago by
Ram
45k
0
votes
0
replies
1.0k
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Comment:
Comment: Cytoscape Diffusion Algorithm
3.5 years ago by
Ram
45k
0
votes
1
reply
7.3k
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Comment:
Comment: Csv. To VCF. File convert
3.5 years ago by
Ram
45k
3
votes
0
replies
2.3k
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Comment:
Comment: GSEA analysis
3.5 years ago by
Ram
45k
0
votes
0
replies
1.7k
views
Comment:
Comment: STAR indexing error: terminate called after throwing an instance of 'std::out_of
3.5 years ago by
Ram
45k
0
votes
0
replies
1.6k
views
Comment:
Comment: Can I use the transcripts_to_genes.txt file from kallisto for bulk RNA seq data?
3.5 years ago by
Ram
45k
0
votes
1
reply
1.6k
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Comment:
Comment: Can I use the transcripts_to_genes.txt file from kallisto for bulk RNA seq data?
3.5 years ago by
Ram
45k
0
votes
1
reply
1.7k
views
Comment:
Comment: STAR indexing error: terminate called after throwing an instance of 'std::out_of
3.5 years ago by
Ram
45k
0
votes
0
replies
544
views
Comment:
Comment: Protonation Tool for DNA
3.5 years ago by
Ram
45k
0
votes
0
replies
1.4k
views
Comment:
Comment: Reference genome, VCF files, genotype
3.5 years ago by
Ram
45k
0
votes
0
replies
1.0k
views
Comment:
Comment: Pathway databases for machine learning
3.5 years ago by
Ram
45k
0
votes
0
replies
946
views
Comment:
Comment: Extract first 3 PC for all confounding variables to be used as covariates
3.5 years ago by
Ram
45k
0
votes
0
replies
1.2k
views
Comment:
Comment: Missing SAM header when piping the samtools mpileup output to a VarScan call
3.5 years ago by
Ram
45k
0
votes
0
replies
4.6k
views
Comment:
Comment: VEP tab/vcf - Different output
3.5 years ago by
Ram
45k
0
votes
1
reply
1.5k
views
Comment:
Comment: Is there a genetic map with centimorgan distance of all SNPs hg19
3.5 years ago by
Ram
45k
0
votes
1
reply
2.0k
views
Comment:
Comment: vcf to txt
3.5 years ago by
Ram
45k
0
votes
0
replies
1.7k
views
Comment:
Comment: Quantify leucine-rich repeats (LRR)
3.5 years ago by
Ram
45k
1
vote
0
replies
3.4k
views
Comment:
Comment: Annotations vep : keep high impact in any transcript + canonical
3.5 years ago by
Ram
45k
2
votes
0
replies
4.3k
views
Comment:
Comment: SQL-why do we need it in Bioinformatics ?
3.5 years ago by
Ram
45k
1
vote
0
replies
3.4k
views
Comment:
Comment: Annotations vep : keep high impact in any transcript + canonical
3.5 years ago by
Ram
45k
0
votes
1
reply
1.3k
views
Comment:
Comment: VCF file comparison and plotting them
3.5 years ago by
Ram
45k
1
vote
2
replies
3.4k
views
Comment:
Comment: Annotations vep : keep high impact in any transcript + canonical
3.5 years ago by
Ram
45k
0
votes
0
replies
3.4k
views
Comment:
Comment: Annotations vep : keep high impact in any transcript + canonical
3.5 years ago by
Ram
45k
1
vote
0
replies
1.3k
views
Comment:
Comment: VCF file comparison and plotting them
3.5 years ago by
Ram
45k
0
votes
0
replies
1.4k
views
Comment:
Comment: Is Tophat 2 good?
3.5 years ago by
Ram
45k
0
votes
0
replies
2.9k
views
Comment:
Comment: highlight subset of cells on tSNE plot
3.5 years ago by
Ram
45k
0
votes
0
replies
1.6k
views
Comment:
Comment: RSeQC - does it make sense to run it on the genome BAM when alignment was to tra
3.5 years ago by
Ram
45k
0
votes
0
replies
1.4k
views
Comment:
Comment: Replace names in FASTA headers from the first white space
3.5 years ago by
Ram
45k
0
votes
1
reply
1.6k
views
Comment:
Comment: RSeQC - does it make sense to run it on the genome BAM when alignment was to tra
3.5 years ago by
Ram
45k
0
votes
1
reply
1.1k
views
Comment:
Comment: Question about analyzing data in high perforfmance computer.
3.5 years ago by
Ram
45k
0
votes
0
replies
2.2k
views
Comment:
Comment: When to merge BAM or SAM files?
3.5 years ago by
Ram
45k
1
vote
1
reply
813
views
Comment:
Comment: Structural annotations of vcf. files
3.5 years ago by
Ram
45k
1
vote
0
replies
912
views
Comment:
Comment: Processing proteomics data
3.5 years ago by
Ram
45k
0
votes
1
reply
1.3k
views
Comment:
Comment: Error message during SNP analysis with KisSplice
3.5 years ago by
Ram
45k
0
votes
0
replies
1.4k
views
Comment:
Comment: Genome index problem
3.5 years ago by
Ram
45k
0
votes
0
replies
2.8k
views
Comment:
Comment: Seurat cluster label transfer
3.5 years ago by
Ram
45k
0
votes
1
reply
1.4k
views
Comment:
Comment: Genome index problem
3.5 years ago by
Ram
45k
1
vote
0
replies
1.6k
views
Comment:
Comment: Data Mining
3.5 years ago by
Ram
45k
1
vote
0
replies
619
views
Comment:
Comment: CNV calls from DNA read counts
3.6 years ago by
Ram
45k
1
vote
1
reply
1.6k
views
Comment:
Comment: Data Mining
3.6 years ago by
Ram
45k
0
votes
0
replies
24k
views
Comment:
Comment: Subsetting a fasta file using seqinr in R
3.6 years ago by
Ram
45k
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