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Answer: Answer: Downloading a huge amount of Fastq files
22 months ago by tomas4482 ▴ 390
2
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0
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481
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Answer: Answer: Why does the CADD database have multiple lines for the same mutation/substitutio
22 months ago by tomas4482 ▴ 390
0
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1
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690
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Answer: Answer: Get nucleotide sequence of assembled RNA transcripts
22 months ago by tomas4482 ▴ 390
1
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0
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413
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gene strand determined by flag in read1 and read2 should be intepreted differently?
samtools RNA-seq bam
updated 10 months ago by 43k • written 22 months ago by ▴ 390
1
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0
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1.9k
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Comment: Comment: how can we count that how many alignments contains a deletion?please guide me
22 months ago by tomas4482 ▴ 390
1
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1
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1.9k
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Answer: Answer: how can we count that how many alignments contains a deletion?please guide me
22 months ago by tomas4482 ▴ 390
3
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0
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392
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Answer: Answer: Colon cancer and single nucleotide variants
22 months ago by tomas4482 ▴ 390
0
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0
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3.7k
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Answer: Answer: STAR alignment getting KILLED in process. Please help!
22 months ago by tomas4482 ▴ 390
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1
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1.2k
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Answer: Answer: Why after normalization of scRNA-Seq data by DESeq2 the p-value of a large numbe
22 months ago by tomas4482 ▴ 390
0
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0
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42k
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Comment: Comment: Get chromosome sizes from fasta file
22 months ago by tomas4482 ▴ 390
1
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0
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932
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Answer: Answer: Seurat dotplot
2.0 years ago by tomas4482 ▴ 390
1
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1
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638
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Does anyone know how to use Human Splicing Finder?
prediction splicing finder HSF human
2.0 years ago by tomas4482 ▴ 390
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0
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638
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Answer: Answer: Does anyone know how to use Human Splicing Finder?
2.0 years ago by tomas4482 ▴ 390
0
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0
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695
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Answer: Answer: Help with adding new ID names to read count
2.1 years ago by tomas4482 ▴ 390
0
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0
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477
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Comment: Comment: How to concatenate samtools output into one single file?
2.1 years ago by tomas4482 ▴ 390
2
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2
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477
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How to concatenate samtools output into one single file?
samtools
updated 10 months ago by 43k • written 2.1 years ago by ▴ 390
1
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0
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393
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Single exon has two distinct PSI in TCGA SpliceSeq.
SpliceSeq alternative splicing skipping exon
2.2 years ago by tomas4482 ▴ 390
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0
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2.7k
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Answer: Answer: BAM file reads mapping to multiple genes
2.4 years ago by tomas4482 ▴ 390
0
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0
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771
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Comment: Comment: integrated scRNA-seq dataset
2.4 years ago by tomas4482 ▴ 390
1
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2
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771
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integrated scRNA-seq dataset
scRNA-seq
updated 2.4 years ago by 8.9k • written 2.5 years ago by ▴ 390
0
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1
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744
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Comment: Comment: GC/AT base content crossed at the tail of read
2.5 years ago by tomas4482 ▴ 390
0
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3
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744
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GC/AT base content crossed at the tail of read
DNA sequence WGS WES
updated 2.5 years ago by 141k • written 2.5 years ago by ▴ 390
1
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7
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2.4k
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featureCounts has low successfully assigned reads
RNA-seq featureCounts
updated 9 months ago by • 0 • written 2.5 years ago by ▴ 390
1
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1
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2.4k
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Answer: Answer: featureCounts has low successfully assigned reads
2.5 years ago by tomas4482 ▴ 390
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0
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3.0k
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Answer: Answer: Base recalibration in normal vs. tumor somatic variant calling in WXS data?
2.5 years ago by tomas4482 ▴ 390
0
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1
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2.4k
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Comment: Comment: featureCounts has low successfully assigned reads
2.5 years ago by tomas4482 ▴ 390
0
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0
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2.4k
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Comment: Comment: featureCounts has low successfully assigned reads
2.5 years ago by tomas4482 ▴ 390
1
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7
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3.7k
views
6 follow
Aspera: Failed to authenticate
ENA aspera
2.5 years ago by tomas4482 ▴ 390
1
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0
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3.7k
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Answer: Answer: Aspera: Failed to authenticate
2.5 years ago by tomas4482 ▴ 390
0
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0
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3.7k
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Comment: Comment: Aspera: Failed to authenticate
2.5 years ago by tomas4482 ▴ 390
0
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1
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681
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Search predicted peptides from proteomes
peptide proteome search
updated 2.6 years ago by ▴ 40 • written 2.6 years ago by ▴ 390
4
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4
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1.6k
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SRA/ENA library layout is inconsistent with the data source
ENA fastq illumina SRA
2.7 years ago by tomas4482 ▴ 390
2
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0
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1.6k
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Answer: Answer: SRA/ENA library layout is inconsistent with the data source
2.7 years ago by tomas4482 ▴ 390
1
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0
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1.6k
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Comment: Comment: SRA/ENA library layout is inconsistent with the data source
2.7 years ago by tomas4482 ▴ 390
1
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0
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1.6k
views
Comment: Comment: SRA/ENA library layout is inconsistent with the data source
2.7 years ago by tomas4482 ▴ 390
1
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1
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860
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Answer: Answer: Single-cell RNA Seq on whole organ or whole tissue with known cell origins
2.7 years ago by tomas4482 ▴ 390
0
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0
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5.7k
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Comment: Comment: How to create interval list from reference fasta or dict file?
2.8 years ago by tomas4482 ▴ 390
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