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Comment:
Comment: Question: Is there a way to reformat vcf 4.3 down to 4.2?
6 months ago by
bounlu
▴ 270
0
votes
1
reply
3.2k
views
Comment:
Comment: counting number of CpGs that are methylated and unmethylated in a read of whole
8 months ago by
bounlu
▴ 270
0
votes
0
replies
2.9k
views
Comment:
Comment: fusion detection for DNA Sequencing data
9 months ago by
bounlu
▴ 270
0
votes
0
replies
1.9k
views
Comment:
Comment: cnvkit Error message "length of weights should be the same as the number of prob
9 months ago by
bounlu
▴ 270
0
votes
0
replies
11k
views
Answer:
Answer: What Is The Meaning Of Snp Strand
12 months ago by
bounlu
▴ 270
0
votes
0
replies
18k
views
Answer:
Answer: How to download dbSNP153 vcf files in hg19/GRCH37 version
12 months ago by
bounlu
▴ 270
0
votes
0
replies
15k
views
Comment:
Comment: MAF vs VAF
15 months ago by
bounlu
▴ 270
0
votes
0
replies
45k
views
Answer:
Answer: Converting a VCF with SNPs and indels to BED format
2.2 years ago by
bounlu
▴ 270
1
vote
1
reply
9.4k
views
Answer:
Answer: Extract UMIs using UMI-tools
10 weeks ago by
bounlu
▴ 270
7
votes
5
replies
8.0k
views
6 follow
How to access GeneCards via XML?
GeneCards
XML
updated 3.4 years ago by
Shicheng Guo
★ 9.6k • written 11.1 years ago by
bounlu
▴ 270
0
votes
0
replies
60k
views
Comment:
Comment: How to extract sample id using bcftools or vcftools
3.9 years ago by
bounlu
▴ 270
0
votes
0
replies
37k
views
Comment:
C: Batch correction in DESeq2
4.5 years ago by
bounlu
▴ 270
1
vote
1
reply
116k
views
Comment:
C: How to plot coverage and depth statistics of a bam file
4.8 years ago by
bounlu
▴ 270
0
votes
0
replies
6.1k
views
Comment:
C: CellRanger Make Counts Expected Cells
4.8 years ago by
bounlu
▴ 270
0
votes
0
replies
13k
views
Comment:
C: correcting for a batch in DESeq2
5.0 years ago by
bounlu
▴ 270
0
votes
0
replies
13k
views
Comment:
C: STAR or Bowtie for small RNA seq?
5.1 years ago by
bounlu
▴ 270
0
votes
1
reply
5.4k
views
Comment:
C: best STAR options for miRNA mapping?
5.1 years ago by
bounlu
▴ 270
1
vote
0
replies
6.3k
views
Comment:
C: Cellranger count fails at mapping
5.1 years ago by
bounlu
▴ 270
0
votes
1
reply
7.1k
views
Answer:
A: software of single-cell RNA-seq from fastq or fasta
5.1 years ago by
bounlu
▴ 270
1
vote
1
reply
16k
views
Comment:
C: How to download mm10 GTF file with the gene id and gene name using UCSC table br
5.3 years ago by
bounlu
▴ 270
0
votes
1
reply
6.0k
views
Comment:
A: How to analyze the RNAseq paired samples with DESeq2?
5.4 years ago by
bounlu
▴ 270
0
votes
0
replies
11k
views
Answer:
A: input for rMATS
5.5 years ago by
bounlu
▴ 270
0
votes
0
replies
9.4k
views
Answer:
A: How to merge multiple single cell sequencing data after processing by CellRanger
5.5 years ago by
bounlu
▴ 270
0
votes
0
replies
57k
views
Answer:
A: Visualization of ChIP-seq data using Heatmaps (Updated: 06/10/16)
5.5 years ago by
bounlu
▴ 270
0
votes
0
replies
1.5k
views
Answer:
A: RNAfold with batch constraints
5.6 years ago by
bounlu
▴ 270
0
votes
0
replies
16k
views
Answer:
A: How to install gdc-client in Ubnutu
5.6 years ago by
bounlu
▴ 270
0
votes
0
replies
1.6k
views
Comment:
C: Find 12-mer not mapping to the human genome
5.7 years ago by
bounlu
▴ 270
0
votes
0
replies
11k
views
Comment:
C: input for rMATS
6.1 years ago by
bounlu
▴ 270
0
votes
0
replies
11k
views
Comment:
C: input for rMATS
6.1 years ago by
bounlu
▴ 270
0
votes
1
reply
11k
views
Comment:
C: input for rMATS
6.1 years ago by
bounlu
▴ 270
0
votes
0
replies
16k
views
Comment:
C: How many genes to include for a GSEA analysis
6.1 years ago by
bounlu
▴ 270
0
votes
1
reply
4.1k
views
Comment:
C: DESeq2: unable to allocate memory error
6.2 years ago by
bounlu
▴ 270
0
votes
0
replies
5.1k
views
Answer:
A: TCGA BRCA sample_type blood derived normal?
6.4 years ago by
bounlu
▴ 270
1
vote
0
replies
5.5k
views
Comment:
C: Getting error in running rMATS
6.5 years ago by
bounlu
▴ 270
5
votes
1
reply
60k
views
Answer:
A: how to extract sample id with bcftools or vcftools
updated 6.6 years ago by
zx8754
12k • written 7.3 years ago by
bounlu
▴ 270
0
votes
0
replies
9.7k
views
Comment:
Comment: Splicing factor database
updated 2.8 years ago by
Ram
45k • written 6.8 years ago by
bounlu
▴ 270
3
votes
1
reply
2.9k
views
circRNA-Seq analysis tools
circRNA-Seq
circrna
updated 6.8 years ago by
IP
▴ 780 • written 6.8 years ago by
bounlu
▴ 270
2
votes
3
replies
1.6k
views
Find 12-mer not mapping to the human genome
mapping
alignment
sequencing
sequence
updated 6.8 years ago by
5heikki
11k • written 6.8 years ago by
bounlu
▴ 270
1
vote
0
replies
79k
views
Comment:
C: VCF files: Change Chromosome Notation
6.9 years ago by
bounlu
▴ 270
1
vote
2
replies
71k
views
Comment:
C: How To Convert Gencode Gtf Into Bed Format ?
7.2 years ago by
bounlu
▴ 270
1
vote
0
replies
3.1k
views
Answer:
A: Training dataset for NGS HLA typing (reads >200bp from PCR amplicons)
7.3 years ago by
bounlu
▴ 270
1
vote
0
replies
20k
views
Answer:
A: Software For Hla Typing Using Ngs?
7.3 years ago by
bounlu
▴ 270
0
votes
0
replies
25k
views
Comment:
C: Bwa Mem Method For Mapping, With Or Without Trimming Reads?
7.4 years ago by
bounlu
▴ 270
0
votes
0
replies
5.7k
views
Comment:
C: Script for analyzing idat (illumina) microarray files with limma, any suggestion
7.4 years ago by
bounlu
▴ 270
0
votes
1
reply
5.7k
views
Comment:
C: Script for analyzing idat (illumina) microarray files with limma, any suggestion
7.5 years ago by
bounlu
▴ 270
0
votes
0
replies
58k
views
Comment:
C: How To Download All Sra Samples At Once ?
7.8 years ago by
bounlu
▴ 270
0
votes
0
replies
31k
views
Comment:
C: Extract Sequence From Fasta File Using Ids From A Separate File
8.1 years ago by
bounlu
▴ 270
2
votes
1
reply
4.4k
views
Homozygous/Heterozygous Deletions (Copy Number Variation) in TCGA
cnv
TCGA
updated 8.3 years ago by
yajunyu172
• 0 • written 11.1 years ago by
bounlu
▴ 270
0
votes
0
replies
16k
views
Comment:
C: FastQ quality check : what can we correct ?
8.6 years ago by
bounlu
▴ 270
0
votes
0
replies
12k
views
Comment:
C: Paired End Trimmomatic producing asymmetric paired read files.
8.8 years ago by
bounlu
▴ 270
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