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5
votes
0
replies
17k
views
Answer:
A: Best Resources To Learn Molecular Biology For A Computer Scientist.
updated 5.2 years ago by
Ram
44k • written 14.1 years ago by
Rm
8.3k
3
votes
0
replies
11k
views
Answer:
A: Illumina Genome Analyzer - Single End Vs Paired End
updated 5.2 years ago by
Ram
44k • written 14.1 years ago by
Rm
8.3k
1
vote
1
reply
4.4k
views
Answer:
A: How To Process Raw Pileup
updated 5.2 years ago by
Ram
44k • written 14.2 years ago by
Rm
8.3k
0
votes
0
replies
4.4k
views
Comment:
C: How To Process Raw Pileup
updated 5.2 years ago by
Ram
44k • written 14.2 years ago by
Rm
8.3k
0
votes
0
replies
4.4k
views
Comment:
C: How To Process Raw Pileup
updated 5.2 years ago by
Ram
44k • written 14.2 years ago by
Rm
8.3k
1
vote
0
replies
9.7k
views
Answer:
Answer: How Do I Map, Align, And Plot My Solid Results?
updated 13 months ago by
Ram
44k • written 14.2 years ago by
Rm
8.3k
2
votes
0
replies
4.9k
views
Answer:
A: Snp Analysis In 454 Sequences
updated 5.2 years ago by
Ram
44k • written 14.1 years ago by
Rm
8.3k
3
votes
2
replies
7.3k
views
Answer:
A: Perl How To Isolate Fasta Sequences With A Range Of Values
updated 5.2 years ago by
Ram
44k • written 14.1 years ago by
Rm
8.3k
6
votes
1
reply
56k
views
Answer:
A: Extracting Multiple Fasta Sequences At A Time From A File Containing Many Sequen
updated 5.2 years ago by
Ram
44k • written 14.1 years ago by
Rm
8.3k
0
votes
1
reply
3.4k
views
Any One Has Sucess With Cuffdiff With Gencode V16 Or V15 Gtf File?
cuffdiff
updated 5.3 years ago by
chenlin_920
• 0 • written 11.6 years ago by
Rm
8.3k
11
votes
5
replies
3.4k
views
Is There A Tool That Can Map Article(S) Citations From Labs On Google Maps Etc?
updated 5.6 years ago by
Biostar
20 • written 11.7 years ago by
Rm
8.3k
12
votes
12
replies
9.2k
views
How To Extract Go Terms From A Given Kegg Id
biomart
kegg
go
updated 5.7 years ago by
Shaurya Jauhari
▴ 50 • written 12.4 years ago by
Rm
8.3k
1
vote
0
replies
1.8k
views
Job:
Postdoctoral Research Position in Neuroimaging and Genomics of Addiction
Neuroimaging
genomics
updated 18 months ago by
Ram
44k • written 6.2 years ago by
Rm
8.3k
1
vote
0
replies
1.2k
views
Job:
Postdoctoral Fellow in Cardiovascular Disease Epidemiology
Exome-sequencing
EHR
updated 17 months ago by
Ram
44k • written 6.1 years ago by
Rm
8.3k
6
votes
0
replies
32k
views
Answer:
A: C/C++ Libraries For Bioinformatics?
updated 6.2 years ago by
Ram
44k • written 14.1 years ago by
Rm
8.3k
3
votes
2
replies
45k
views
Answer:
A: How To Generate A Consensus Fasta Sequence From Sam Tools Pileup?
updated 6.2 years ago by
Ram
44k • written 14.2 years ago by
Rm
8.3k
0
votes
1
reply
11k
views
Comment:
C: How To Download All Est Sequences For Organism Xx From Ncbi?
updated 6.2 years ago by
Ram
44k • written 11.3 years ago by
Rm
8.3k
6
votes
2
replies
76k
views
Answer:
A: How To Remove The Same Sequences In The Fasta Files?
updated 6.2 years ago by
Ram
44k • written 14.0 years ago by
Rm
8.3k
3
votes
14
replies
2.4k
views
6 follow
Forum:
Search for gene variants
next-gen
updated 18 months ago by
Ram
44k • written 6.3 years ago by
Rm
8.3k
0
votes
1
reply
2.4k
views
Comment:
C: Search for gene variants
6.3 years ago by
Rm
8.3k
0
votes
0
replies
2.4k
views
Comment:
C: Search for gene variants
6.3 years ago by
Rm
8.3k
0
votes
1
reply
2.4k
views
Comment:
C: Search for gene variants
6.3 years ago by
Rm
8.3k
0
votes
1
reply
2.4k
views
Comment:
C: Google search for gene variants
6.3 years ago by
Rm
8.3k
0
votes
2
replies
2.4k
views
Comment:
C: Google search for gene variants
6.3 years ago by
Rm
8.3k
0
votes
0
replies
3.4k
views
Comment:
C: PRSice: Imputation and clumping
6.3 years ago by
Rm
8.3k
5
votes
1
reply
252k
views
Answer:
A: Tools To Calculate Average Coverage For A Bam File?
updated 6.3 years ago by
Ram
44k • written 13.4 years ago by
Rm
8.3k
0
votes
0
replies
5.2k
views
Comment:
C: Is there an API for querying the Exac database?
6.5 years ago by
Rm
8.3k
1
vote
0
replies
29k
views
Answer:
C: Get gene names from rs SNP ids
updated 6.6 years ago by
zx8754
12k • written 10.2 years ago by
Rm
8.3k
0
votes
0
replies
5.0k
views
Comment:
C: Does A Bwa Bam File Contain Entries For All Unaligned Paired-End Reads?
updated 7.0 years ago by
h.mon
35k • written 13.2 years ago by
Rm
8.3k
0
votes
0
replies
1.7k
views
Comment:
A: Has someone any experience with hmmvar and hmmvar-func?
7.0 years ago by
Rm
8.3k
39
votes
16
replies
39k
views
7 follow
Efficient And Fastest Way To Sort Large (>100Gb) Bam Files?
sort
bam
samtools
picard
updated 2.9 years ago by
Ram
44k • written 12.7 years ago by
Rm
8.3k
6
votes
3
replies
3.5k
views
Human+Viral Genomes In A Single Index (Bwa Or Other Aligners)
human
genome
index
bwa
bowtie
updated 7.5 years ago by
Biostar
20 • written 13.1 years ago by
Rm
8.3k
0
votes
0
replies
2.6k
views
Comment:
C: GTEx: Genotypes specifc differential gene expression plot for an RSID?
8.3 years ago by
Rm
8.3k
0
votes
1
reply
2.6k
views
Comment:
C: GTEx: Genotypes specifc differential gene expression plot for an RSID?
8.3 years ago by
Rm
8.3k
1
vote
4
replies
2.6k
views
GTEx: Genotypes specifc differential gene expression plot for an RSID?
GTEx
API
R
updated 8.3 years ago by
WouterDeCoster
47k • written 8.3 years ago by
Rm
8.3k
0
votes
0
replies
6.5k
views
Comment:
C: Reproduction GTex Box plot
8.3 years ago by
Rm
8.3k
0
votes
0
replies
4.2k
views
Comment:
C: Significance of PLINK epistasis p-values
8.4 years ago by
Rm
8.3k
4
votes
4
replies
4.4k
views
Suggest Pirna Ngs Small Rna Analysis Pipelines/Workflows
workflow
updated 8.5 years ago by
opplatek
▴ 300 • written 11.1 years ago by
Rm
8.3k
12
votes
16
replies
27k
views
9 follow
How To Export Normalized Counts From Edger
edger
counts
updated 2.9 years ago by
Ram
44k • written 12.1 years ago by
Rm
8.3k
0
votes
2
replies
4.3k
views
Samtools-0.1.18: Samtools View Filtering Based On Chromosome Reports Wrong Output
samtools
bam
updated 8.6 years ago by
Biostar
20 • written 12.3 years ago by
Rm
8.3k
0
votes
1
reply
3.0k
views
How To Use Rsem With Soapdenovo-Trans
trinity
rna-seq
updated 8.8 years ago by
kanika.151
▴ 160 • written 12.5 years ago by
Rm
8.3k
0
votes
0
replies
5.6k
views
Comment:
Comment: Transcript support level in Gencode gtf v19
updated 2.4 years ago by
Ram
44k • written 8.8 years ago by
Rm
8.3k
0
votes
0
replies
3.2k
views
Job:
Postdoctoral Fellow (Genetics & Bioinformatics) (#24714) @ Geisinger Health System -- Danville, PA (US)
next-gen
germline
ngs
updated 2.3 years ago by
Ram
44k • written 8.9 years ago by
Rm
8.3k
3
votes
2
replies
2.8k
views
Download link to ensembl human GRCH37 transcript support level (TSL) flags information?
ensembl
TSL
updated 2.3 years ago by
Ram
44k • written 8.9 years ago by
Rm
8.3k
0
votes
0
replies
5.1k
views
Comment:
C: Drawing Pfam Domain Architecture Of Many Uniprot Ids
9.0 years ago by
Rm
8.3k
0
votes
1
reply
45k
views
Comment:
Comment: How To Create Mutation Diagram In R Or In Any Tools?
updated 2.2 years ago by
Ram
44k • written 9.2 years ago by
Rm
8.3k
3
votes
2
replies
1.8k
views
Need recommendations for Family aware Variant/indel caller for WGS data
famseq
updated 2.1 years ago by
Ram
44k • written 9.3 years ago by
Rm
8.3k
0
votes
0
replies
3.4k
views
Comment:
Comment: Named variants to Rsids or coordinates or Haplotype?
updated 23 months ago by
Ram
44k • written 9.4 years ago by
Rm
8.3k
0
votes
1
reply
3.4k
views
Comment:
Comment: Named variants to Rsids or coordinates or Haplotype?
updated 23 months ago by
Ram
44k • written 9.5 years ago by
Rm
8.3k
0
votes
1
reply
3.4k
views
Comment:
Comment: Named variants to Rsids or coordinates or Haplotype?
updated 23 months ago by
Ram
44k • written 9.5 years ago by
Rm
8.3k
596 results • Page
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