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Comment: C: RNA-SeQC error no output
updated 5.5 years ago by 45k • written 10.2 years ago by ▴ 370
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0
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10k
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Comment: C: featureCounts isoform vs gene summarization
updated 5.6 years ago by 45k • written 9.6 years ago by ▴ 370
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1
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10k
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Answer: A: featureCounts isoform vs gene summarization
updated 5.6 years ago by 45k • written 9.6 years ago by ▴ 370
5
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13k
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Answer: A: featureCounts exon counting problem
updated 5.6 years ago by 45k • written 9.6 years ago by ▴ 370
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0
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6.3k
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Answer: A: questions about TruSeq Adapter
updated 5.6 years ago by 45k • written 9.7 years ago by ▴ 370
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1
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7.7k
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Answer: A: txt file to bigwig
updated 5.6 years ago by 45k • written 9.7 years ago by ▴ 370
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4.1k
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Answer: Answer: Splicing programs to find alternative polyadenylation
updated 3.3 years ago by 45k • written 9.7 years ago by ▴ 370
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0
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7.7k
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Comment: C: txt file to bigwig
updated 5.6 years ago by 45k • written 9.7 years ago by ▴ 370
0
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1
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7.9k
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Comment: C: GFFutils very slow at creating database file. Any Idea why..?
updated 5.7 years ago by 45k • written 10.0 years ago by ▴ 370
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0
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7.9k
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Comment: C: GFFutils very slow at creating database file. Any Idea why..?
updated 5.7 years ago by 45k • written 10.0 years ago by ▴ 370
0
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0
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7.9k
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Comment: C: GFFutils very slow at creating database file. Any Idea why..?
updated 5.7 years ago by 45k • written 10.0 years ago by ▴ 370
0
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0
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4.3k
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Comment: C: Assembling a chromosome for an E. coli strain using contigs/scaffolds from two W
updated 5.7 years ago by 45k • written 10.0 years ago by ▴ 370
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1
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3.2k
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Answer: A: RNASeqQC - Low number of genes detected on run
updated 5.7 years ago by 45k • written 10.1 years ago by ▴ 370
0
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1
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3.8k
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Comment: C: mm9 RNA-seq reference genome
6.8 years ago by Kirill Tsyganov ▴ 370
1
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0
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3.9k
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Comment: C: How to create PCA plot and heatmaps using only significant genes in edgeR ?
6.8 years ago by Kirill Tsyganov ▴ 370
2
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0
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2.6k
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Comment: C: EdgeR analysis with different biological replicates numbers problem
6.8 years ago by Kirill Tsyganov ▴ 370
19
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11
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18k
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SAMtools mpileup and bcftools doesn't call InDels...
SNP INDELs samtools-mpileup variant-calling
updated 2.6 years ago by 45k • written 10.1 years ago by ▴ 370
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0
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18k
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Comment: C: SAMtools mpileup and bcftools doesn't call InDels...
8.3 years ago by Kirill Tsyganov ▴ 370
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0
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2.3k
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Comment: C: Observed and expected fastq header count different when merging two fastq files
9.7 years ago by Kirill Tsyganov ▴ 370
0
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1
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7.9k
views
Comment: Comment: GFFutils very slow at creating database file. Any Idea why..?
updated 2.7 years ago by 45k • written 9.9 years ago by ▴ 370
2
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10
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7.9k
views
GFFutils very slow at creating database file. Any Idea why..?
gffutils gff
updated 2.7 years ago by 45k • written 10.0 years ago by ▴ 370
0
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1
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7.9k
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Comment: Comment: GFFutils very slow at creating database file. Any Idea why..?
updated 2.7 years ago by 45k • written 10.0 years ago by ▴ 370
0
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1
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18k
views
Comment: C: SAMtools mpileup and bcftools doesn't call InDels...
10.1 years ago by Kirill Tsyganov ▴ 370
0
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1
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18k
views
Comment: Comment: SAMtools mpileup and bcftools doesn't call InDels...
updated 2.6 years ago by 45k • written 10.1 years ago by ▴ 370
0
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0
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7.2k
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Comment: Comment: Error in SNP calling using samtools and bcftools
updated 2.6 years ago by 45k • written 10.1 years ago by ▴ 370
0
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0
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2.5k
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Comment: Comment: Where to get human 3'-UTR multiple sequence alignment ?
updated 2.6 years ago by 45k • written 10.1 years ago by ▴ 370
0
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1
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2.6k
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Comment: Comment: Reporting alleles sequences for Amplicon sequencing after variant calling
updated 2.6 years ago by 45k • written 10.1 years ago by ▴ 370
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0
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3.2k
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Comment: Comment: RNASeqQC - Low number of genes detected on run
updated 2.5 years ago by 45k • written 10.1 years ago by ▴ 370
0
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0
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4.8k
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Comment: C: How do I load more than 200 nucleotide EST sequences into fasta files from NCBI
10.1 years ago by Kirill Tsyganov ▴ 370
0
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1
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4.8k
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Comment: Comment: How do I load more than 200 nucleotide EST sequences into fasta files from NCBI
updated 2.5 years ago by 45k • written 10.1 years ago by ▴ 370
0
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1
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4.8k
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Comment: Comment: BWA-mem read mapping depends on chromosome order
updated 2.5 years ago by 45k • written 10.1 years ago by ▴ 370
1
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1
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4.8k
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Comment: C: How do I load more than 200 nucleotide EST sequences into fasta files from NCBI
10.1 years ago by Kirill Tsyganov ▴ 370
0
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0
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4.7k
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Comment: Comment: Obtaining sequence from Bioproject IDs using biopython gives unknown sequence
updated 2.5 years ago by 45k • written 10.1 years ago by ▴ 370
0
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1
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4.7k
views
Answer: Answer: Obtaining sequence from Bioproject IDs using biopython gives unknown sequence
updated 2.5 years ago by 45k • written 10.1 years ago by ▴ 370
0
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0
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11k
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Comment: Comment: Samtools mpileup quality scores all zero
updated 2.5 years ago by 45k • written 10.1 years ago by ▴ 370
3
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2
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11k
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Answer: Answer: Samtools mpileup quality scores all zero
updated 2.5 years ago by 45k • written 10.1 years ago by ▴ 370
2
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1
reply
7.8k
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Answer: Answer: Where to Download & File Format of Reference Gene Annotation for C. elegans WS22
updated 2.8 years ago by 45k • written 10.1 years ago by ▴ 370
0
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0
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5.2k
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Comment: Comment: How to annotate a VCF with Entrez Gene IDs
updated 2.5 years ago by 45k • written 10.1 years ago by ▴ 370
0
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0
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3.4k
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Comment: C: Filter paired reads from samtools
10.1 years ago by Kirill Tsyganov ▴ 370
0
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1
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3.4k
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Comment: Comment: Filter paired reads from samtools
updated 2.5 years ago by 45k • written 10.1 years ago by ▴ 370
0
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0
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5.6k
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Comment: Comment: Python: How to find coordinates of short sequences in a FASTA file?
updated 2.5 years ago by 45k • written 10.2 years ago by ▴ 370
0
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0
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12k
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Comment: C: GTF format: isn't the tag "transcript_id" mandatory?
updated 10.2 years ago by 24k • written 10.2 years ago by ▴ 370
4
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1
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12k
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Answer: Answer: Ensembl GTF format: isn't the tag "transcript_id" mandatory?
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 370
0
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0
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3.2k
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Comment: C: Pairwise Alignment, Biopython : Bio.pairwise2
10.2 years ago by Kirill Tsyganov ▴ 370
0
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0
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3.2k
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Comment: C: Pairwise Alignment, Biopython : Bio.pairwise2
10.2 years ago by Kirill Tsyganov ▴ 370
5
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0
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5.4k
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Answer: Answer: Gff to fasta: Sort and extract sub-feature sequences from fasta in python
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 370
1
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0
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12k
views
Comment: Comment: Ensembl GTF format: isn't the tag "transcript_id" mandatory?
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 370
0
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1
reply
12k
views
Comment: Comment: Ensembl GTF format: isn't the tag "transcript_id" mandatory?
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 370
0
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1
reply
9.2k
views
Answer: Answer: RNA-SeQC error no output
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 370
4
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2
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9.9k
views
What is the best practice for BAM sorting?
RNA-Seq samtools STAR
updated 2.3 years ago by 45k • written 10.3 years ago by ▴ 370
51 results • Page 1 of 2
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