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1
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546
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Comment:
Comment: 99.9999% of Q30 bases is normal?
8 days ago by
MatthewP
★ 1.4k
0
votes
1
reply
397
views
Comment:
Comment: A c library for reading and writing sequences in fasta and fastq format.
6 weeks ago by
MatthewP
★ 1.4k
1
vote
2
replies
1.2k
views
Comment:
Comment: Some lines are not well organized in BED file, how to correct them ? Thanks a lo
3 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
2.2k
views
Comment:
Comment: Should I use the basecaller Dorado to analyze my Nanopore Data?
4 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
392
views
Comment:
Comment: MSA using ggtree msaplot
4 months ago by
MatthewP
★ 1.4k
10
votes
6
replies
5.7k
views
How to create interval list from reference fasta or dict file?
GATK
updated 4 months ago by
Manuel Sokolov Ravasqueira
▴ 100 • written 3.2 years ago by
MatthewP
★ 1.4k
2
votes
1
reply
405
views
Answer:
Answer: Help with gatk CreateSequenceDictionary
updated 4 months ago by
GenoMax
141k • written 4 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
498
views
Comment:
Comment: ANNOVAR Error: All variants in a VCF register as "invalid genotype records in in
4 months ago by
MatthewP
★ 1.4k
0
votes
1
reply
498
views
Comment:
Comment: ANNOVAR Error: All variants in a VCF register as "invalid genotype records in in
5 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
778
views
Comment:
Comment: What is the new Entrez login for NCBI API?
6 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
522
views
Comment:
Comment: How to deal with reads which CIGAR is [0-9]+S
6 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
530
views
Comment:
Comment: What is a tool to get the genome build of a VCF?
6 months ago by
MatthewP
★ 1.4k
1
vote
1
reply
829
views
Comment:
Comment: how to solve the problem "Invalid character (+) in sequence"
8 months ago by
MatthewP
★ 1.4k
1
vote
1
reply
855
views
Comment:
Comment: How to make chromVAR plot?
9 months ago by
MatthewP
★ 1.4k
0
votes
1
reply
987
views
Comment:
Comment: All question mark quality scores on several studies
10 months ago by
MatthewP
★ 1.4k
0
votes
1
reply
987
views
Comment:
Comment: All question mark quality scores on several studies
10 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
1.0k
views
Comment:
Comment: OTU, ASV and Kraken2
10 months ago by
MatthewP
★ 1.4k
0
votes
1
reply
987
views
Comment:
Comment: All question mark quality scores on several studies
10 months ago by
MatthewP
★ 1.4k
0
votes
1
reply
1.5k
views
Comment:
Comment: End to End Solution for Multiple Sequence Alignment on Fasta Files in Python
10 months ago by
MatthewP
★ 1.4k
1
vote
0
replies
413
views
Comment:
Comment: weird behaviour on bedtools
10 months ago by
MatthewP
★ 1.4k
1
vote
1
reply
1.1k
views
Answer:
Answer: how to use nohup with parallel
10 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
658
views
Answer:
Answer: Can we get fastq read id of certain species that kraken assigned?
11 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
669
views
Comment:
Comment: Comparing variant calls
12 months ago by
MatthewP
★ 1.4k
0
votes
1
reply
3.0k
views
Comment:
Comment: gseKEGG - no gene can be mapped (RNAseq analysis)
13 months ago by
MatthewP
★ 1.4k
0
votes
1
reply
1.4k
views
Comment:
Comment: R:scheduled cores 1, 5 did not deliver results
14 months ago by
MatthewP
★ 1.4k
1
vote
1
reply
576
views
Answer:
Answer: Multiple sequence alignment of mtDNA HV1-3 in R
14 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
2.6k
views
Comment:
Comment: MSA visualization python package for sequence analysis
17 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
752
views
Comment:
Comment: How can Biostrings calculate consensus sequence without counting gaps?
18 months ago by
MatthewP
★ 1.4k
0
votes
2
replies
752
views
How can Biostrings calculate consensus sequence without counting gaps?
Biostrings
alignment
18 months ago by
MatthewP
★ 1.4k
2
votes
1
reply
788
views
Comment:
Comment: HISAT2 running issue (output getting slower)
19 months ago by
MatthewP
★ 1.4k
4
votes
0
replies
972
views
Answer:
Answer: Loading reference genome from BSgenome
20 months ago by
MatthewP
★ 1.4k
2
votes
3
replies
3.0k
views
How to keep sample name while using samtools mpileup + varscan to do variant call?
samtools
mpileup
varscan
updated 21 months ago by
GenoMax
141k • written 5.8 years ago by
MatthewP
★ 1.4k
0
votes
1
reply
1.6k
views
Comment:
Comment: Set up conda rna seq analysis
21 months ago by
MatthewP
★ 1.4k
0
votes
1
reply
1.6k
views
Comment:
Comment: Set up conda rna seq analysis
21 months ago by
MatthewP
★ 1.4k
1
vote
1
reply
1.6k
views
Comment:
Comment: bowtie2 error "Unable to read file magic number"
22 months ago by
MatthewP
★ 1.4k
0
votes
0
replies
968
views
Comment:
Comment: How to handle 2 peaks in fastQC GC plot...
22 months ago by
MatthewP
★ 1.4k
2
votes
5
replies
2.8k
views
Some questions about call variants for mtDNA using GATK HaplotypeCaller
GATK
HaplotypeCaller
mtDNA
updated 23 months ago by
kanika.151
▴ 130 • written 5.6 years ago by
MatthewP
★ 1.4k
0
votes
0
replies
928
views
Comment:
Comment: featureCounts stuck
2.1 years ago by
MatthewP
★ 1.4k
0
votes
1
reply
1.6k
views
Comment:
Comment: How to do pathway enrichment analysis with genomic ranges data (ATAC-Seq peaks)?
2.2 years ago by
MatthewP
★ 1.4k
4
votes
5
replies
1.6k
views
How to do pathway enrichment analysis with genomic ranges data (ATAC-Seq peaks)?
ATAC-Seq
pathway
annotation
updated 2.1 years ago by
LauferVA
4.2k • written 2.2 years ago by
MatthewP
★ 1.4k
1
vote
0
replies
2.9k
views
Comment:
Comment: DiffBind missing peaks and FRiP
2.2 years ago by
MatthewP
★ 1.4k
0
votes
0
replies
334
views
Do I need to remove ATAC-Seq large peaks?
ATAC-Seq
Genrich
2.2 years ago by
MatthewP
★ 1.4k
0
votes
0
replies
1.6k
views
Comment:
Comment: Bedtools genomecov - Bam to bedgraph conversion
2.4 years ago by
MatthewP
★ 1.4k
1
vote
0
replies
2.8k
views
Answer:
Answer: Interpreting GISTIC2 output
2.4 years ago by
MatthewP
★ 1.4k
0
votes
0
replies
1.5k
views
Answer:
Answer: GATK Mutect2 errors during basic variant calling
2.4 years ago by
MatthewP
★ 1.4k
0
votes
1
reply
1.5k
views
Comment:
Comment: Best practice for running GATK VQSR on X chromosome
2.4 years ago by
MatthewP
★ 1.4k
0
votes
1
reply
1.7k
views
Comment:
Comment: featureCounts low annotation rate RNA-seq
2.5 years ago by
MatthewP
★ 1.4k
0
votes
1
reply
1.7k
views
Comment:
Comment: featureCounts low annotation rate RNA-seq
2.5 years ago by
MatthewP
★ 1.4k
0
votes
1
reply
1.7k
views
Answer:
Answer: featureCounts low annotation rate RNA-seq
2.5 years ago by
MatthewP
★ 1.4k
0
votes
0
replies
1.5k
views
Answer:
Answer: How maftools oncoplot classifies variant classifications
2.5 years ago by
MatthewP
★ 1.4k
274 results • Page
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