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comments
0
votes
0
replies
443
views
Comment:
Comment: cancer type prediction based on RNASeq gene expression data?
5 months ago by
J.F.Jiang
▴ 930
1
vote
2
replies
443
views
cancer type prediction based on RNASeq gene expression data?
cancer
RNA-seq
updated 5 months ago by
Ram
44k • written 5 months ago by
J.F.Jiang
▴ 930
20
votes
11
replies
15k
views
10 follow
How Can We Find The Info For 3'Utr And 5'Utr In Gencode Gtf File?
utr
updated 7 months ago by
cmdcolin
★ 4.0k • written 11.3 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
485
views
Any tool that can give me a list of DNA/RNA aptamers against specific protein as the in vitro SELEX library to screen the sequences?
aptamer
protein
SELEX
8 months ago by
J.F.Jiang
▴ 930
0
votes
1
reply
611
views
tumor fraction estimation and fragment size plot using sWGS data
ctDNA
NGS
WGS
updated 12 months ago by
Ram
44k • written 2.0 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
793
views
Comment:
Comment: BCR/TCR analysis using target capture sequencing data
18 months ago by
J.F.Jiang
▴ 930
0
votes
2
replies
793
views
BCR/TCR analysis using target capture sequencing data
capture
ngs
TCR
BCR
18 months ago by
J.F.Jiang
▴ 930
0
votes
1
reply
1.3k
views
Comment:
Comment: combine/merge closet variants into one from mutect2
18 months ago by
J.F.Jiang
▴ 930
0
votes
1
reply
1.3k
views
Comment:
Comment: combine/merge closet variants into one from mutect2
18 months ago by
J.F.Jiang
▴ 930
0
votes
5
replies
1.3k
views
combine/merge closet variants into one from mutect2
variants
mutect2
merge
gatk
updated 18 months ago by
Istvan Albert
101k • written 18 months ago by
J.F.Jiang
▴ 930
0
votes
1
reply
867
views
Comment:
Comment: BCL2 fusions not detected in RNA level
18 months ago by
J.F.Jiang
▴ 930
0
votes
4
replies
867
views
BCL2 fusions not detected in RNA level
fusion
RNA
BCL2
updated 18 months ago by
ATpoint
85k • written 18 months ago by
J.F.Jiang
▴ 930
0
votes
0
replies
488
views
multiplex pcr PRIMER
sequence
primer
multiplex
pcr
20 months ago by
J.F.Jiang
▴ 930
0
votes
0
replies
409
views
heterozygosity control from NGS data
heterozygosity
NGS
SNP
2.2 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
1.1k
views
Comment:
Comment: tumor fraction estimation for ctDNA panel sequecing data
2.7 years ago by
J.F.Jiang
▴ 930
1
vote
3
replies
1.1k
views
tumor fraction estimation for ctDNA panel sequecing data
fraction
NGS
panel
tumor
ctDNA
updated 2.7 years ago by
markus.riester
▴ 550 • written 2.7 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
807
views
hgvs annotation from VCF
VCF
HGVS
annotation
updated 2.7 years ago by
cpad0112
21k • written 2.7 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
447
views
any tool to plot the fragment profile for ctDNA samples?
fragment
ctDNA
2.8 years ago by
J.F.Jiang
▴ 930
4
votes
10
replies
9.3k
views
6 follow
GATK HaolotypeCaller takes too much time for variant calling
HaplotypeCaller
GATK
updated 7 months ago by
Ram
44k • written 7.0 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
884
views
genomewide CNV analysis and plot from low pass WGS data
CNV
CNVSEQ
WGS
3.8 years ago by
J.F.Jiang
▴ 930
0
votes
4
replies
1.1k
views
public tools to distinguish germline variants from somatic ones in NGS data without matched normal
germline
somatic
NGS
tumor
updated 3.9 years ago by
Biostar
20 • written 4.0 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
1.1k
views
Comment:
C: public tools to distinguish germline variants from somatic ones in NGS data with
4.0 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
1.1k
views
Comment:
C: public tools to distinguish germline variants from somatic ones in NGS data with
4.0 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
831
views
best tool to evaluate the CNV status of germline samples using 1x WGS
CNV
WGS
4.1 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
734
views
Max mutation allele frequency against tumor purity
tumor
AF
PURITY
4.2 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
1.1k
views
Comment:
C: HPV EBV typing from cancer genome data
4.3 years ago by
J.F.Jiang
▴ 930
2
votes
4
replies
1.1k
views
HPV EBV typing from cancer genome data
HPV
EBV
NGS
updated 4.3 years ago by
d-cameron
★ 2.9k • written 4.3 years ago by
J.F.Jiang
▴ 930
32
votes
12
replies
24k
views
9 follow
Bwa Mem Method For Mapping, With Or Without Trimming Reads?
bwa
updated 4.3 years ago by
Biostar
20 • written 10.9 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
1.1k
views
LOH segment inferring from WES data for germline sample
LOH
WES
4.5 years ago by
J.F.Jiang
▴ 930
1
vote
6
replies
2.4k
views
fusion detection for DNA Sequencing data
fusion
NGS
DNA
updated 10 weeks ago by
Ă–mer An
▴ 260 • written 4.6 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
2.4k
views
Comment:
C: fusion detection for DNA Sequencing data
4.6 years ago by
J.F.Jiang
▴ 930
1
vote
0
replies
2.4k
views
Comment:
C: fusion detection for DNA Sequencing data
4.6 years ago by
J.F.Jiang
▴ 930
1
vote
0
replies
1.7k
views
Comment:
C: CNV analysis for tumor panel
4.6 years ago by
J.F.Jiang
▴ 930
1
vote
1
reply
752
views
looking somatic variants interpreter, AS CKB database
ckb
somatic
interpreter
updated 4.7 years ago by
Kevin Blighe
88k • written 4.8 years ago by
J.F.Jiang
▴ 930
2
votes
5
replies
2.9k
views
remove primer sequences from BAM file
bam
primer
updated 4.9 years ago by
hongen.hugo.xu
• 0 • written 6.3 years ago by
J.F.Jiang
▴ 930
0
votes
2
replies
1.1k
views
convenient tools to collect target mapping metrics
target
mapping
updated 4.9 years ago by
Biostar
20 • written 5.0 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
1.1k
views
Comment:
C: convenient tools to collect target mapping metrics
5.0 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
1.1k
views
calculate MSI STATUS using predefined MSI loci
MSI
msisensor
5.1 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
24k
views
Comment:
C: Bwa Mem Method For Mapping, With Or Without Trimming Reads?
updated 5.1 years ago by
Ram
44k • written 10.9 years ago by
J.F.Jiang
▴ 930
2
votes
5
replies
1.7k
views
CNV analysis for tumor panel
CNV
updated 5.3 years ago by
Eric T.
★ 2.8k • written 5.3 years ago by
J.F.Jiang
▴ 930
1
vote
5
replies
3.1k
views
amplicon based germline CNV caller
amplicon
germline
CNV
updated 5.3 years ago by
lffu_0032
▴ 90 • written 7.3 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
1.7k
views
Comment:
A: CNV analysis for tumor panel
5.3 years ago by
J.F.Jiang
▴ 930
0
votes
2
replies
1.5k
views
pairwise calculation of relationship based on selected SNPs with MAF>0.3
relationship
SNP
updated 5.9 years ago by
Biostar
20 • written 7.0 years ago by
J.F.Jiang
▴ 930
3
votes
3
replies
2.3k
views
Simulate genotypes for SNPs, considering MAF and LD structure
genotype
simulation
SNP
MAF
LD
updated 6.0 years ago by
zx8754
12k • written 6.9 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
2.7k
views
Comment:
C: Free Genetic Genealogy Software
6.3 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
2.9k
views
Comment:
C: remove primer sequences from BAM file
6.3 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
2.9k
views
Comment:
C: remove primer sequences from BAM file
updated 6.3 years ago by
WouterDeCoster
47k • written 6.3 years ago by
J.F.Jiang
▴ 930
0
votes
2
replies
1.9k
views
autosomal ancestry inference
GWAS
ancestry
updated 6.3 years ago by
Kevin Blighe
88k • written 6.3 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
1.8k
views
how to genotype given SNP alleles from NGS data using freebayes
genotype
NGS
freebayes
updated 6.9 years ago by
ines.sanchezdonoso
• 0 • written 7.2 years ago by
J.F.Jiang
▴ 930
0
votes
0
replies
1.8k
views
Comment:
C: extract region bam
7.0 years ago by
J.F.Jiang
▴ 930
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