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393
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Comment:
Comment: Identify and count gaps in sam/bam files
20 days ago by
Mark
★ 1.5k
1
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1
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232
views
Comment:
Comment: What does evidence of batch effect in bulk rnaseq look like?
22 days ago by
Mark
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0
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0
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213
views
Comment:
Comment: best tools for bacterial wgMLST
22 days ago by
Mark
★ 1.5k
0
votes
0
replies
393
views
Comment:
Comment: Identify and count gaps in sam/bam files
22 days ago by
Mark
★ 1.5k
0
votes
2
replies
657
views
Comment:
Comment: Multiple sequence alignment images
5 months ago by
Mark
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0
votes
1
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657
views
Comment:
Comment: Multiple sequence alignment images
5 months ago by
Mark
★ 1.5k
0
votes
1
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709
views
Comment:
Comment: What tools exist for filtering hundreds of VCFs (and annotated into VCFs in txt
6 months ago by
Mark
★ 1.5k
0
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0
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436
views
Comment:
Comment: How to Design a Segmented RNA Virus Vector
8 months ago by
Mark
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0
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0
replies
19k
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Answer:
Answer: How to count fasta sequences efficiently using (or not ) biopython
8 months ago by
Mark
★ 1.5k
0
votes
0
replies
897
views
Comment:
Comment: Annoate complex heatmap columns
9 months ago by
Mark
★ 1.5k
0
votes
0
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676
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Comment:
Comment: To draw a heatmap displaying DEGs associated with a specific KEGG pathway.
9 months ago by
Mark
★ 1.5k
0
votes
0
replies
1.5k
views
Comment:
Comment: Annotating Proteins in heatmap with 1 or more pathways using R.
9 months ago by
Mark
★ 1.5k
0
votes
0
replies
894
views
Comment:
Comment: vcf.gz to vcf
9 months ago by
Mark
★ 1.5k
1
vote
1
reply
1.5k
views
Comment:
Comment: Annotating Proteins in heatmap with 1 or more pathways using R.
9 months ago by
Mark
★ 1.5k
0
votes
0
replies
359
views
Comment:
Comment: RepBase database for help
9 months ago by
Mark
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0
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0
replies
893
views
Comment:
Comment: Why 99% coverage at 20X depth for sequencing?
9 months ago by
Mark
★ 1.5k
1
vote
1
reply
1.5k
views
Comment:
Comment: Annotating Proteins in heatmap with 1 or more pathways using R.
9 months ago by
Mark
★ 1.5k
0
votes
1
reply
1.1k
views
Comment:
Comment: Filtering a 10X generated .bam file based on a list of barcodes
9 months ago by
Mark
★ 1.5k
2
votes
0
replies
827
views
Comment:
Comment: Visualization package for Maf Files using Python
9 months ago by
Mark
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0
votes
1
reply
1.2k
views
Comment:
Comment: Aligner with statistics included?
9 months ago by
Mark
★ 1.5k
0
votes
1
reply
893
views
Comment:
Comment: Why 99% at 20X for sequencing?
9 months ago by
Mark
★ 1.5k
0
votes
2
replies
1.1k
views
Comment:
Comment: Filtering a 10X generated .bam file based on a list of barcodes
9 months ago by
Mark
★ 1.5k
1
vote
1
reply
1.5k
views
Comment:
Comment: Annotating Proteins in heatmap with 1 or more pathways using R.
9 months ago by
Mark
★ 1.5k
1
vote
0
replies
1.5k
views
Comment:
Comment: Annotating Proteins in heatmap with 1 or more pathways using R.
9 months ago by
Mark
★ 1.5k
2
votes
1
reply
1.5k
views
Answer:
Answer: Annotating Proteins in heatmap with 1 or more pathways using R.
9 months ago by
Mark
★ 1.5k
1
vote
1
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2.3k
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Comment:
Comment: Which alignment for whole bacterial genomes for phylogenetic tree?
9 months ago by
Mark
★ 1.5k
1
vote
1
reply
1.5k
views
Comment:
Comment: Annotating Proteins in heatmap with 1 or more pathways using R.
9 months ago by
Mark
★ 1.5k
1
vote
0
replies
1.0k
views
Answer:
Answer: GSEApy plot TypeError
updated 8 months ago by
Ram
44k • written 9 months ago by
Mark
★ 1.5k
0
votes
0
replies
1.3k
views
Answer:
Answer: Extract compounds/proteins from genomic data
9 months ago by
Mark
★ 1.5k
0
votes
0
replies
629
views
Comment:
Comment: How to read tsv data as dgcmatrix
9 months ago by
Mark
★ 1.5k
1
vote
0
replies
866
views
Comment:
Comment: how to get to a VCF from bam files
9 months ago by
Mark
★ 1.5k
1
vote
1
reply
911
views
Comment:
Comment: KEGG Pathway analysis for non-model organism using goseq
9 months ago by
Mark
★ 1.5k
0
votes
1
reply
957
views
Comment:
Comment: pyDESeq2 Index Error?
9 months ago by
Mark
★ 1.5k
1
vote
0
replies
569
views
Answer:
Answer: Visualization of Genomes
9 months ago by
Mark
★ 1.5k
2
votes
1
reply
894
views
Answer:
Answer: vcf.gz to vcf
10 months ago by
Mark
★ 1.5k
1
vote
0
replies
690
views
Answer:
Answer: How to get ncol = nrow?
updated 9 months ago by
Ram
44k • written 10 months ago by
Mark
★ 1.5k
0
votes
0
replies
929
views
Comment:
Comment: Viewing chromatograms on linux
10 months ago by
Mark
★ 1.5k
2
votes
0
replies
929
views
Answer:
Answer: Viewing chromatograms on linux
10 months ago by
Mark
★ 1.5k
2
votes
0
replies
14k
views
Answer:
Answer: find positions of a short sequence in a genome
11 months ago by
Mark
★ 1.5k
0
votes
0
replies
2.0k
views
Comment:
Comment: Problem with mamba/conda install
12 months ago by
Mark
★ 1.5k
0
votes
1
reply
517
views
Comment:
Comment: Chewbbaca - explanation of the output
12 months ago by
Mark
★ 1.5k
1
vote
0
replies
690
views
Comment:
Comment: Download rRNAs.fasta for all bacteria from database
12 months ago by
Mark
★ 1.5k
0
votes
0
replies
1.6k
views
Comment:
Comment: I want to rename sequence headers
12 months ago by
Mark
★ 1.5k
1
vote
0
replies
886
views
Answer:
Answer: Best pipeline / resources / tools for whole genome assembly
12 months ago by
Mark
★ 1.5k
3
votes
2
replies
1.3k
views
Answer:
Answer: adding features to gtf file using agat tool function
12 months ago by
Mark
★ 1.5k
1
vote
1
reply
1.6k
views
Answer:
Answer: I want to rename sequence headers
12 months ago by
Mark
★ 1.5k
0
votes
1
reply
742
views
Comment:
Comment: How do I calculate differential expression for RNA-seq values with the "limma" p
13 months ago by
Mark
★ 1.5k
0
votes
0
replies
1.1k
views
Comment:
Comment: Reorder GO terms using R
13 months ago by
Mark
★ 1.5k
0
votes
1
reply
695
views
Answer:
Answer: how to look at interaction between SNP and gene
16 months ago by
Mark
★ 1.5k
1
vote
0
replies
725
views
Answer:
Answer: Remove part of headers in FASTA file
16 months ago by
Mark
★ 1.5k
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