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5
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0
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16k
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Answer: A: Best Resources To Learn Molecular Biology For A Computer Scientist.
updated 4.6 years ago by 43k • written 13.5 years ago by 8.3k
3
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0
replies
11k
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Answer: A: Illumina Genome Analyzer - Single End Vs Paired End
updated 4.6 years ago by 43k • written 13.5 years ago by 8.3k
1
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1
reply
4.1k
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Answer: A: How To Process Raw Pileup
updated 4.6 years ago by 43k • written 13.6 years ago by 8.3k
0
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0
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4.1k
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Comment: C: How To Process Raw Pileup
updated 4.6 years ago by 43k • written 13.6 years ago by 8.3k
0
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0
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4.1k
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Comment: C: How To Process Raw Pileup
updated 4.6 years ago by 43k • written 13.6 years ago by 8.3k
1
vote
0
replies
9.3k
views
Answer: Answer: How Do I Map, Align, And Plot My Solid Results?
updated 6 months ago by 43k • written 13.6 years ago by 8.3k
2
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0
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4.4k
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Answer: A: Snp Analysis In 454 Sequences
updated 4.7 years ago by 43k • written 13.5 years ago by 8.3k
3
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2
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6.9k
views
Answer: A: Perl How To Isolate Fasta Sequences With A Range Of Values
updated 4.7 years ago by 43k • written 13.6 years ago by 8.3k
6
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1
reply
55k
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Answer: A: Extracting Multiple Fasta Sequences At A Time From A File Containing Many Sequen
updated 4.7 years ago by 43k • written 13.6 years ago by 8.3k
0
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1
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3.3k
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Any One Has Sucess With Cuffdiff With Gencode V16 Or V15 Gtf File?
cuffdiff
updated 4.7 years ago by • 0 • written 11.0 years ago by 8.3k
11
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5
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3.2k
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Is There A Tool That Can Map Article(S) Citations From Labs On Google Maps Etc?
updated 5.0 years ago by 20 • written 11.2 years ago by 8.3k
12
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12
replies
8.3k
views
How To Extract Go Terms From A Given Kegg Id
biomart kegg go
updated 5.2 years ago by ▴ 50 • written 11.8 years ago by 8.3k
0
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0
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1.7k
views
Job: Postdoctoral Research Position in Neuroimaging and Genomics of Addiction
Neuroimaging genomics
updated 11 months ago by 43k • written 5.6 years ago by 8.3k
1
vote
0
replies
1.2k
views
Job: Postdoctoral Fellow in Cardiovascular Disease Epidemiology
Exome-sequencing EHR
updated 10 months ago by 43k • written 5.6 years ago by 8.3k
6
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0
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30k
views
Answer: A: C/C++ Libraries For Bioinformatics?
updated 5.6 years ago by 43k • written 13.5 years ago by 8.3k
3
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2
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44k
views
Answer: A: How To Generate A Consensus Fasta Sequence From Sam Tools Pileup?
updated 5.6 years ago by 43k • written 13.6 years ago by 8.3k
0
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1
reply
10k
views
Comment: C: How To Download All Est Sequences For Organism Xx From Ncbi?
updated 5.6 years ago by 43k • written 10.8 years ago by 8.3k
6
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2
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73k
views
Answer: A: How To Remove The Same Sequences In The Fasta Files?
updated 5.7 years ago by 43k • written 13.5 years ago by 8.3k
3
votes
14
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2.1k
views
6 follow
Forum: Search for gene variants
next-gen
updated 11 months ago by 43k • written 5.7 years ago by 8.3k
0
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1
reply
2.1k
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Comment: C: Search for gene variants
5.7 years ago by Rm 8.3k
0
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0
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2.1k
views
Comment: C: Search for gene variants
5.7 years ago by Rm 8.3k
0
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1
reply
2.1k
views
Comment: C: Search for gene variants
5.7 years ago by Rm 8.3k
0
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1
reply
2.1k
views
Comment: C: Google search for gene variants
5.7 years ago by Rm 8.3k
0
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2
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2.1k
views
Comment: C: Google search for gene variants
5.7 years ago by Rm 8.3k
0
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0
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3.2k
views
Comment: C: PRSice: Imputation and clumping
5.7 years ago by Rm 8.3k
5
votes
1
reply
239k
views
Answer: A: Tools To Calculate Average Coverage For A Bam File?
updated 5.7 years ago by 43k • written 12.8 years ago by 8.3k
0
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0
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5.0k
views
Comment: C: Is there an API for querying the Exac database?
5.9 years ago by Rm 8.3k
1
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0
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27k
views
Answer: C: Get gene names from rs SNP ids
updated 6.0 years ago by 11k • written 9.6 years ago by 8.3k
0
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0
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4.8k
views
Comment: C: Does A Bwa Bam File Contain Entries For All Unaligned Paired-End Reads?
updated 6.4 years ago by 35k • written 12.6 years ago by 8.3k
0
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0
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1.6k
views
Comment: A: Has someone any experience with hmmvar and hmmvar-func?
6.4 years ago by Rm 8.3k
39
votes
16
replies
38k
views
7 follow
Efficient And Fastest Way To Sort Large (>100Gb) Bam Files?
sort bam samtools picard
updated 2.3 years ago by 43k • written 12.1 years ago by 8.3k
6
votes
3
replies
3.3k
views
Human+Viral Genomes In A Single Index (Bwa Or Other Aligners)
human genome index bwa bowtie
updated 6.9 years ago by 20 • written 12.5 years ago by 8.3k
0
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0
replies
2.5k
views
Comment: C: GTEx: Genotypes specifc differential gene expression plot for an RSID?
7.7 years ago by Rm 8.3k
0
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1
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2.5k
views
Comment: C: GTEx: Genotypes specifc differential gene expression plot for an RSID?
7.7 years ago by Rm 8.3k
1
vote
4
replies
2.5k
views
GTEx: Genotypes specifc differential gene expression plot for an RSID?
GTEx API R
updated 7.7 years ago by 47k • written 7.7 years ago by 8.3k
0
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0
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6.3k
views
Comment: C: Reproduction GTex Box plot
7.7 years ago by Rm 8.3k
0
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0
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4.0k
views
Comment: C: Significance of PLINK epistasis p-values
7.8 years ago by Rm 8.3k
4
votes
4
replies
4.2k
views
Suggest Pirna Ngs Small Rna Analysis Pipelines/Workflows
workflow
updated 7.9 years ago by ▴ 290 • written 10.5 years ago by 8.3k
12
votes
16
replies
26k
views
9 follow
How To Export Normalized Counts From Edger
edger counts
updated 2.3 years ago by 43k • written 11.5 years ago by 8.3k
0
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2
replies
4.2k
views
Samtools-0.1.18: Samtools View Filtering Based On Chromosome Reports Wrong Output
samtools bam
updated 8.0 years ago by 20 • written 11.8 years ago by 8.3k
0
votes
1
reply
2.9k
views
How To Use Rsem With Soapdenovo-Trans
trinity rna-seq
updated 8.2 years ago by ▴ 130 • written 12.0 years ago by 8.3k
0
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0
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5.3k
views
Comment: Comment: Transcript support level in Gencode gtf v19
updated 21 months ago by 43k • written 8.2 years ago by 8.3k
0
votes
0
replies
3.0k
views
Job: Postdoctoral Fellow (Genetics & Bioinformatics) (#24714) @ Geisinger Health System -- Danville, PA (US)
next-gen germline ngs
updated 21 months ago by 43k • written 8.3 years ago by 8.3k
3
votes
2
replies
2.6k
views
Download link to ensembl human GRCH37 transcript support level (TSL) flags information?
ensembl TSL
updated 21 months ago by 43k • written 8.3 years ago by 8.3k
0
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0
replies
4.9k
views
Comment: C: Drawing Pfam Domain Architecture Of Many Uniprot Ids
8.4 years ago by Rm 8.3k
0
votes
1
reply
43k
views
Comment: Comment: How To Create Mutation Diagram In R Or In Any Tools?
updated 19 months ago by 43k • written 8.7 years ago by 8.3k
3
votes
2
replies
1.6k
views
Need recommendations for Family aware Variant/indel caller for WGS data
famseq
updated 18 months ago by 43k • written 8.7 years ago by 8.3k
0
votes
0
replies
3.2k
views
Comment: Comment: Named variants to Rsids or coordinates or Haplotype?
updated 16 months ago by 43k • written 8.9 years ago by 8.3k
0
votes
1
reply
3.2k
views
Comment: Comment: Named variants to Rsids or coordinates or Haplotype?
updated 16 months ago by 43k • written 8.9 years ago by 8.3k
0
votes
1
reply
3.2k
views
Comment: Comment: Named variants to Rsids or coordinates or Haplotype?
updated 16 months ago by 43k • written 8.9 years ago by 8.3k
596 results • Page 2 of 12
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