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5
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0
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18k
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Answer: A: Best Resources To Learn Molecular Biology For A Computer Scientist.
updated 6.2 years ago by 45k • written 15.0 years ago by 8.3k
3
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0
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12k
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Answer: A: Illumina Genome Analyzer - Single End Vs Paired End
updated 6.2 years ago by 45k • written 15.0 years ago by 8.3k
1
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1
reply
5.1k
views
Answer: A: How To Process Raw Pileup
updated 6.2 years ago by 45k • written 15.1 years ago by 8.3k
0
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0
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5.1k
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Comment: C: How To Process Raw Pileup
updated 6.2 years ago by 45k • written 15.1 years ago by 8.3k
0
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0
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5.1k
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Comment: C: How To Process Raw Pileup
updated 6.2 years ago by 45k • written 15.1 years ago by 8.3k
1
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0
replies
11k
views
Answer: Answer: How Do I Map, Align, And Plot My Solid Results?
updated 2.0 years ago by 45k • written 15.1 years ago by 8.3k
2
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0
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5.6k
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Answer: A: Snp Analysis In 454 Sequences
updated 6.2 years ago by 45k • written 15.0 years ago by 8.3k
3
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2
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8.8k
views
Answer: A: Perl How To Isolate Fasta Sequences With A Range Of Values
updated 6.2 years ago by 45k • written 15.1 years ago by 8.3k
6
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1
reply
59k
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Answer: A: Extracting Multiple Fasta Sequences At A Time From A File Containing Many Sequen
updated 6.2 years ago by 45k • written 15.1 years ago by 8.3k
0
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1
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3.7k
views
Any One Has Sucess With Cuffdiff With Gencode V16 Or V15 Gtf File?
cuffdiff
updated 6.2 years ago by • 0 • written 12.5 years ago by 8.3k
11
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5
replies
3.8k
views
Is There A Tool That Can Map Article(S) Citations From Labs On Google Maps Etc?
updated 6.5 years ago by 20 • written 12.7 years ago by 8.3k
12
votes
12
replies
11k
views
How To Extract Go Terms From A Given Kegg Id
biomart kegg go
updated 6.7 years ago by ▴ 50 • written 13.3 years ago by 8.3k
1
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0
replies
2.0k
views
Job: Postdoctoral Research Position in Neuroimaging and Genomics of Addiction
Neuroimaging genomics
updated 2.4 years ago by 45k • written 7.1 years ago by 8.3k
1
vote
0
replies
1.5k
views
Job: Postdoctoral Fellow in Cardiovascular Disease Epidemiology
Exome-sequencing EHR
updated 2.4 years ago by 45k • written 7.1 years ago by 8.3k
6
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0
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35k
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Answer: A: C/C++ Libraries For Bioinformatics?
updated 7.1 years ago by 45k • written 15.0 years ago by 8.3k
3
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2
replies
48k
views
Answer: A: How To Generate A Consensus Fasta Sequence From Sam Tools Pileup?
updated 7.1 years ago by 45k • written 15.1 years ago by 8.3k
0
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1
reply
12k
views
Comment: C: How To Download All Est Sequences For Organism Xx From Ncbi?
updated 7.2 years ago by 45k • written 12.3 years ago by 8.3k
6
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2
replies
81k
views
Answer: A: How To Remove The Same Sequences In The Fasta Files?
updated 7.2 years ago by 45k • written 15.0 years ago by 8.3k
3
votes
14
replies
3.4k
views
6 follow
Forum: Search for gene variants
next-gen
updated 2.4 years ago by 45k • written 7.2 years ago by 8.3k
0
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1
reply
3.4k
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Comment: C: Search for gene variants
7.2 years ago by Rm 8.3k
0
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0
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3.4k
views
Comment: C: Search for gene variants
7.2 years ago by Rm 8.3k
0
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1
reply
3.4k
views
Comment: C: Search for gene variants
7.2 years ago by Rm 8.3k
0
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1
reply
3.4k
views
Comment: C: Google search for gene variants
7.2 years ago by Rm 8.3k
0
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2
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3.4k
views
Comment: C: Google search for gene variants
7.2 years ago by Rm 8.3k
0
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0
replies
3.9k
views
Comment: C: PRSice: Imputation and clumping
7.2 years ago by Rm 8.3k
5
votes
1
reply
269k
views
Answer: A: Tools To Calculate Average Coverage For A Bam File?
updated 7.2 years ago by 45k • written 14.3 years ago by 8.3k
0
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0
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5.8k
views
Comment: C: Is there an API for querying the Exac database?
7.4 years ago by Rm 8.3k
1
vote
0
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31k
views
Answer: C: Get gene names from rs SNP ids
updated 7.6 years ago by 12k • written 11.1 years ago by 8.3k
0
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0
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5.5k
views
Comment: C: Does A Bwa Bam File Contain Entries For All Unaligned Paired-End Reads?
updated 7.9 years ago by 35k • written 14.1 years ago by 8.3k
0
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0
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2.1k
views
Comment: A: Has someone any experience with hmmvar and hmmvar-func?
7.9 years ago by Rm 8.3k
39
votes
16
replies
41k
views
7 follow
Efficient And Fastest Way To Sort Large (>100Gb) Bam Files?
sort bam samtools picard
updated 3.8 years ago by 45k • written 13.6 years ago by 8.3k
6
votes
3
replies
4.0k
views
Human+Viral Genomes In A Single Index (Bwa Or Other Aligners)
human genome index bwa bowtie
updated 8.4 years ago by 20 • written 14.0 years ago by 8.3k
0
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0
replies
3.2k
views
Comment: C: GTEx: Genotypes specifc differential gene expression plot for an RSID?
9.2 years ago by Rm 8.3k
0
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1
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3.2k
views
Comment: C: GTEx: Genotypes specifc differential gene expression plot for an RSID?
9.2 years ago by Rm 8.3k
1
vote
4
replies
3.2k
views
GTEx: Genotypes specifc differential gene expression plot for an RSID?
GTEx API R
updated 9.2 years ago by 48k • written 9.2 years ago by 8.3k
0
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0
replies
7.4k
views
Comment: C: Reproduction GTex Box plot
9.2 years ago by Rm 8.3k
0
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0
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4.7k
views
Comment: C: Significance of PLINK epistasis p-values
9.4 years ago by Rm 8.3k
4
votes
4
replies
5.0k
views
Suggest Pirna Ngs Small Rna Analysis Pipelines/Workflows
workflow
updated 9.4 years ago by ▴ 300 • written 12.0 years ago by 8.3k
12
votes
16
replies
28k
views
9 follow
How To Export Normalized Counts From Edger
edger counts
updated 3.8 years ago by 45k • written 13.1 years ago by 8.3k
0
votes
2
replies
4.6k
views
Samtools-0.1.18: Samtools View Filtering Based On Chromosome Reports Wrong Output
samtools bam
updated 9.6 years ago by 20 • written 13.3 years ago by 8.3k
0
votes
1
reply
3.3k
views
How To Use Rsem With Soapdenovo-Trans
trinity rna-seq
updated 9.7 years ago by ▴ 160 • written 13.5 years ago by 8.3k
0
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0
replies
6.6k
views
Comment: Comment: Transcript support level in Gencode gtf v19
updated 3.3 years ago by 45k • written 9.7 years ago by 8.3k
0
votes
0
replies
3.6k
views
Job: Postdoctoral Fellow (Genetics & Bioinformatics) (#24714) @ Geisinger Health System -- Danville, PA (US)
next-gen germline ngs
updated 3.2 years ago by 45k • written 9.8 years ago by 8.3k
3
votes
2
replies
3.2k
views
Download link to ensembl human GRCH37 transcript support level (TSL) flags information?
ensembl TSL
updated 3.2 years ago by 45k • written 9.8 years ago by 8.3k
0
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0
replies
5.8k
views
Comment: C: Drawing Pfam Domain Architecture Of Many Uniprot Ids
10.0 years ago by Rm 8.3k
0
votes
1
reply
49k
views
Comment: Comment: How To Create Mutation Diagram In R Or In Any Tools?
updated 3.1 years ago by 45k • written 10.2 years ago by 8.3k
3
votes
2
replies
2.1k
views
Need recommendations for Family aware Variant/indel caller for WGS data
famseq
updated 3.0 years ago by 45k • written 10.3 years ago by 8.3k
0
votes
0
replies
4.5k
views
Comment: Comment: Named variants to Rsids or coordinates or Haplotype?
updated 2.8 years ago by 45k • written 10.4 years ago by 8.3k
0
votes
1
reply
4.5k
views
Comment: Comment: Named variants to Rsids or coordinates or Haplotype?
updated 2.8 years ago by 45k • written 10.4 years ago by 8.3k
0
votes
1
reply
4.5k
views
Comment: Comment: Named variants to Rsids or coordinates or Haplotype?
updated 2.8 years ago by 45k • written 10.4 years ago by 8.3k
596 results • Page 2 of 12
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