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comments
3
votes
6
replies
4.5k
views
6 follow
Parse FASTQC data
NGS
updated 2.0 years ago by
pcsk9
• 0 • written 6.9 years ago by
win
▴ 990
0
votes
0
replies
1.7k
views
VCF with SnpEff and gene name annotations
VCF
6.9 years ago by
win
▴ 990
6
votes
6
replies
5.6k
views
Determine Variant Location From Vcf
vcf
updated 6.9 years ago by
Biostar
20 • written 12.3 years ago by
win
▴ 990
1
vote
1
reply
1.1k
views
PICARD tools param database
PICARD
updated 6.9 years ago by
Raony GuimarĂ£es
★ 1.4k • written 6.9 years ago by
win
▴ 990
0
votes
2
replies
2.9k
views
Detect CNVs in single sample using cn.MOPS
cn.mops
CNV
updated 7.0 years ago by
colindaven
7.0k • written 8.9 years ago by
win
▴ 990
0
votes
0
replies
1.8k
views
Comment:
C: Microbial genomics pipelines
7.3 years ago by
win
▴ 990
0
votes
1
reply
1.8k
views
Comment:
C: Microbial genomics pipelines
7.3 years ago by
win
▴ 990
1
vote
4
replies
1.8k
views
Microbial genomics pipelines
ngs
microbial genomics
updated 7.3 years ago by
h.mon
35k • written 7.3 years ago by
win
▴ 990
9
votes
10
replies
18k
views
7 follow
Annotate A Vcf File
vcf
annotation
updated 7.6 years ago by
k.kathirvel93
▴ 310 • written 11.2 years ago by
win
▴ 990
1
vote
0
replies
991
views
Disease risk variants from 23andme
variants
7.6 years ago by
win
▴ 990
8
votes
8
replies
8.2k
views
Individual VCF files from main VCF file
VCF
updated 2.6 years ago by
Ram
44k • written 9.8 years ago by
win
▴ 990
0
votes
0
replies
2.2k
views
Comment:
C: Commonly used charts in NGS/ bioinformatics
8.0 years ago by
win
▴ 990
0
votes
1
reply
2.2k
views
Comment:
C: Commonly used charts in NGS/ bioinformatics
8.0 years ago by
win
▴ 990
4
votes
7
replies
2.2k
views
Commonly used charts in NGS/ bioinformatics
sequencing
R
updated 8.0 years ago by
lakhujanivijay
5.9k • written 8.0 years ago by
win
▴ 990
6
votes
2
replies
3.3k
views
Variation Count Based On Chromosome
vcf
updated 8.0 years ago by
Biostar
20 • written 11.0 years ago by
win
▴ 990
0
votes
2
replies
2.7k
views
KEGG REST API
KEGG
updated 8.1 years ago by
lelle
▴ 830 • written 8.1 years ago by
win
▴ 990
0
votes
3
replies
1.3k
views
Variation name pathogenic
next-gen
8.1 years ago by
win
▴ 990
0
votes
1
reply
1.3k
views
Answer:
A: Variation name pathogenic
8.1 years ago by
win
▴ 990
1
vote
8
replies
7.7k
views
Homozygous Ref Calls And No Calls
updated 8.3 years ago by
Korsocius
▴ 260 • written 12.4 years ago by
win
▴ 990
0
votes
0
replies
2.2k
views
ClinVar view from API
ClinVar
8.3 years ago by
win
▴ 990
0
votes
0
replies
1.4k
views
CNVKit for cancer germline mutation detection
NGS
8.4 years ago by
win
▴ 990
0
votes
1
reply
3.8k
views
Comment:
C: cnvkit example data
8.4 years ago by
win
▴ 990
1
vote
0
replies
1.6k
views
Tumor germline CNA caller- concensus
CNA
CNV
NGS
8.4 years ago by
win
▴ 990
0
votes
0
replies
2.0k
views
Comment:
C: Downstream cancer variant reporting
8.4 years ago by
win
▴ 990
12
votes
13
replies
2.0k
views
Downstream cancer variant reporting
ngs
updated 8.4 years ago by
Khader Shameer
18k • written 8.5 years ago by
win
▴ 990
0
votes
0
replies
2.0k
views
Answer:
A: Downstream cancer variant reporting
8.4 years ago by
win
▴ 990
0
votes
1
reply
2.0k
views
Comment:
C: Downstream cancer variant reporting
8.5 years ago by
win
▴ 990
0
votes
1
reply
2.0k
views
Comment:
C: Downstream cancer variant reporting
8.5 years ago by
win
▴ 990
2
votes
4
replies
3.3k
views
Cancer CNV workflow
NGS
updated 8.5 years ago by
ivivek_ngs
★ 5.2k • written 8.5 years ago by
win
▴ 990
0
votes
0
replies
3.3k
views
Comment:
C: Cancer CNV workflow
8.5 years ago by
win
▴ 990
1
vote
1
reply
5.0k
views
HapMap in VCF format
HapMap
updated 8.5 years ago by
andrew.j.skelton73
6.6k • written 8.5 years ago by
win
▴ 990
3
votes
2
replies
5.7k
views
Human GRCh38 and dbSNP VCF and GATK
NGS
updated 8.5 years ago by
Carlos Borroto
★ 2.1k • written 8.5 years ago by
win
▴ 990
0
votes
2
replies
1.7k
views
how to "dope" a FASTQ file with known variants
FASTQ
updated 8.6 years ago by
WouterDeCoster
47k • written 8.6 years ago by
win
▴ 990
0
votes
2
replies
1.5k
views
ACMG Gene List variations
NGS
updated 8.6 years ago by
Ibrahim Tanyalcin
★ 1.2k • written 8.6 years ago by
win
▴ 990
0
votes
0
replies
4.1k
views
Comment:
C: ClinVar local install
8.6 years ago by
win
▴ 990
0
votes
1
reply
4.1k
views
Comment:
C: ClinVar local install
8.6 years ago by
win
▴ 990
2
votes
9
replies
4.1k
views
ClinVar local install
ClinVar
updated 8.6 years ago by
DG
7.3k • written 8.6 years ago by
win
▴ 990
0
votes
0
replies
4.1k
views
Comment:
C: ClinVar local install
8.6 years ago by
win
▴ 990
0
votes
1
reply
4.1k
views
Comment:
C: ClinVar local install
8.6 years ago by
win
▴ 990
0
votes
0
replies
1.2k
views
Common analysis methods for bioinformatics
genomics
proteomics
8.7 years ago by
win
▴ 990
0
votes
1
reply
2.1k
views
Deblock a VCF
VCF
updated 9.5 years ago by
Nicola Casiraghi
▴ 500 • written 9.6 years ago by
win
▴ 990
0
votes
0
replies
15k
views
Comment:
C: Split a VCF file into individual sample files
9.6 years ago by
win
▴ 990
0
votes
1
reply
3.9k
views
Comment:
Comment: HG18 coordinates of rs#
updated 2.4 years ago by
Ram
44k • written 9.6 years ago by
win
▴ 990
0
votes
1
reply
3.9k
views
Comment:
C: HG18 coordinates of rs#
9.6 years ago by
win
▴ 990
2
votes
5
replies
3.9k
views
HG18 coordinates of rs#
dbSNP
updated 2.4 years ago by
Ram
44k • written 9.6 years ago by
win
▴ 990
0
votes
1
reply
2.6k
views
Comment:
Comment: Microarray to VCF
updated 2.4 years ago by
Ram
44k • written 9.6 years ago by
win
▴ 990
0
votes
4
replies
2.6k
views
Microarray to VCF
VCF
updated 2.4 years ago by
Ram
44k • written 9.6 years ago by
win
▴ 990
0
votes
1
reply
24k
views
Comment:
C: Lift-over on a VCF
9.6 years ago by
win
▴ 990
0
votes
1
reply
2.2k
views
FASTQ file names meaning at this link
FASTQ
updated 2.4 years ago by
Ram
44k • written 9.6 years ago by
win
▴ 990
0
votes
1
reply
4.2k
views
Comment:
C: BAM to individual chromosome fasta/fastq
9.6 years ago by
win
▴ 990
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