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Comment:
Comment: counting number of CpGs that are methylated and unmethylated in a read of whole
6 weeks ago by
Ömer An
▴ 260
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0
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2.4k
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Comment:
Comment: fusion detection for DNA Sequencing data
8 weeks ago by
Ömer An
▴ 260
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votes
0
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1.6k
views
Comment:
Comment: cnvkit Error message "length of weights should be the same as the number of prob
10 weeks ago by
Ömer An
▴ 260
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0
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9.9k
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Answer:
Answer: What Is The Meaning Of Snp Strand
5 months ago by
Ömer An
▴ 260
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0
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16k
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Answer:
Answer: How to download dbSNP153 vcf files in hg19/GRCH37 version
5 months ago by
Ömer An
▴ 260
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0
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14k
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Comment:
Comment: MAF vs VAF
7 months ago by
Ömer An
▴ 260
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0
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41k
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Answer:
Answer: Converting a VCF with SNPs and indels to BED format
19 months ago by
Ömer An
▴ 260
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1
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6.6k
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Answer:
Answer: Extract UMIs using UMI-tools
23 months ago by
Ömer An
▴ 260
7
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5
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7.1k
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6 follow
How to access GeneCards via XML?
GeneCards
XML
updated 2.8 years ago by
Shicheng Guo
★ 9.5k • written 10.5 years ago by
Ömer An
▴ 260
0
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0
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56k
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Comment:
Comment: How to extract sample id using bcftools or vcftools
3.3 years ago by
Ömer An
▴ 260
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0
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33k
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Comment:
C: Batch correction in DESeq2
3.9 years ago by
Ömer An
▴ 260
1
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1
reply
109k
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Comment:
C: How to plot coverage and depth statistics of a bam file
4.2 years ago by
Ömer An
▴ 260
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5.5k
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Comment:
C: CellRanger Make Counts Expected Cells
4.2 years ago by
Ömer An
▴ 260
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0
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12k
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Comment:
C: correcting for a batch in DESeq2
4.3 years ago by
Ömer An
▴ 260
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0
replies
12k
views
Comment:
C: STAR or Bowtie for small RNA seq?
4.5 years ago by
Ömer An
▴ 260
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1
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5.0k
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Comment:
C: best STAR options for miRNA mapping?
4.5 years ago by
Ömer An
▴ 260
1
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5.7k
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Comment:
C: Cellranger count fails at mapping
4.5 years ago by
Ömer An
▴ 260
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1
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6.2k
views
Answer:
A: software of single-cell RNA-seq from fastq or fasta
4.5 years ago by
Ömer An
▴ 260
1
vote
1
reply
14k
views
Comment:
C: How to download mm10 GTF file with the gene id and gene name using UCSC table br
4.7 years ago by
Ömer An
▴ 260
0
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1
reply
5.1k
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Comment:
A: How to analyze the RNAseq paired samples with DESeq2?
4.8 years ago by
Ömer An
▴ 260
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0
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9.7k
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Answer:
A: input for rMATS
4.9 years ago by
Ömer An
▴ 260
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0
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8.7k
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Answer:
A: How to merge multiple single cell sequencing data after processing by CellRanger
4.9 years ago by
Ömer An
▴ 260
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0
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53k
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Answer:
A: Visualization of ChIP-seq data using Heatmaps (Updated: 06/10/16)
4.9 years ago by
Ömer An
▴ 260
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0
replies
1.3k
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Answer:
A: RNAfold with batch constraints
5.0 years ago by
Ömer An
▴ 260
0
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0
replies
14k
views
Answer:
A: How to install gdc-client in Ubnutu
5.0 years ago by
Ömer An
▴ 260
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0
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1.4k
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Comment:
C: Find 12-mer not mapping to the human genome
5.1 years ago by
Ömer An
▴ 260
0
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0
replies
9.7k
views
Comment:
C: input for rMATS
5.4 years ago by
Ömer An
▴ 260
0
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0
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9.7k
views
Comment:
C: input for rMATS
5.4 years ago by
Ömer An
▴ 260
0
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1
reply
9.7k
views
Comment:
C: input for rMATS
5.4 years ago by
Ömer An
▴ 260
0
votes
0
replies
14k
views
Comment:
C: How many genes to include for a GSEA analysis
5.5 years ago by
Ömer An
▴ 260
0
votes
1
reply
3.5k
views
Comment:
C: DESeq2: unable to allocate memory error
5.6 years ago by
Ömer An
▴ 260
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0
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4.9k
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Answer:
A: TCGA BRCA sample_type blood derived normal?
5.7 years ago by
Ömer An
▴ 260
1
vote
0
replies
5.1k
views
Comment:
C: Getting error in running rMATS
5.9 years ago by
Ömer An
▴ 260
5
votes
1
reply
56k
views
Answer:
A: how to extract sample id with bcftools or vcftools
updated 6.0 years ago by
zx8754
12k • written 6.7 years ago by
Ömer An
▴ 260
0
votes
0
replies
9.1k
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Comment:
Comment: Splicing factor database
updated 2.2 years ago by
Ram
44k • written 6.2 years ago by
Ömer An
▴ 260
1
vote
1
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2.6k
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circRNA-Seq analysis tools
circRNA-Seq
circrna
updated 6.2 years ago by
IP
▴ 770 • written 6.2 years ago by
Ömer An
▴ 260
2
votes
3
replies
1.4k
views
Find 12-mer not mapping to the human genome
mapping
alignment
sequencing
sequence
updated 6.2 years ago by
5heikki
11k • written 6.2 years ago by
Ömer An
▴ 260
1
vote
0
replies
72k
views
Comment:
C: VCF files: Change Chromosome Notation
6.2 years ago by
Ömer An
▴ 260
1
vote
2
replies
67k
views
Comment:
C: How To Convert Gencode Gtf Into Bed Format ?
6.6 years ago by
Ömer An
▴ 260
1
vote
0
replies
2.8k
views
Answer:
A: Training dataset for NGS HLA typing (reads >200bp from PCR amplicons)
6.7 years ago by
Ömer An
▴ 260
1
vote
0
replies
19k
views
Answer:
A: Software For Hla Typing Using Ngs?
6.7 years ago by
Ömer An
▴ 260
0
votes
0
replies
24k
views
Comment:
C: Bwa Mem Method For Mapping, With Or Without Trimming Reads?
6.7 years ago by
Ömer An
▴ 260
0
votes
0
replies
5.1k
views
Comment:
C: Script for analyzing idat (illumina) microarray files with limma, any suggestion
6.8 years ago by
Ömer An
▴ 260
0
votes
1
reply
5.1k
views
Comment:
C: Script for analyzing idat (illumina) microarray files with limma, any suggestion
6.9 years ago by
Ömer An
▴ 260
0
votes
0
replies
56k
views
Comment:
C: How To Download All Sra Samples At Once ?
7.2 years ago by
Ömer An
▴ 260
0
votes
0
replies
30k
views
Comment:
C: Extract Sequence From Fasta File Using Ids From A Separate File
7.5 years ago by
Ömer An
▴ 260
2
votes
1
reply
4.3k
views
Homozygous/Heterozygous Deletions (Copy Number Variation) in TCGA
cnv
TCGA
updated 7.7 years ago by
yajunyu172
• 0 • written 10.5 years ago by
Ömer An
▴ 260
0
votes
0
replies
15k
views
Comment:
C: FastQ quality check : what can we correct ?
7.9 years ago by
Ömer An
▴ 260
0
votes
0
replies
11k
views
Comment:
C: Paired End Trimmomatic producing asymmetric paired read files.
8.2 years ago by
Ömer An
▴ 260
1
vote
0
replies
101k
views
Comment:
C: Survival analysis of TCGA patients integrating gene expression (RNASeq) data
8.5 years ago by
Ömer An
▴ 260
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