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2
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16k
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Answer: A: Number of Threads for BWA MEM
6.9 years ago by Raony Guimarães ★ 1.4k
0
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1
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2.2k
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Comment: C: Is it possible to do enrichment analysis for selected genes just with GO number
6.9 years ago by Raony Guimarães ★ 1.4k
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1.6k
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Answer: A: SNP single end read
6.9 years ago by Raony Guimarães ★ 1.4k
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4.8k
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Comment: C: What is the expected rate of SNPs within a human exome sequencing with HiSeq?
6.9 years ago by Raony Guimarães ★ 1.4k
1
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1
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3.2k
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Comment: C: Announcing bioSyntax: Syntax highlighting for biological files
6.9 years ago by Raony Guimarães ★ 1.4k
1
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1.1k
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Answer: A: PICARD tools param database
6.9 years ago by Raony Guimarães ★ 1.4k
3
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1
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2.6k
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Answer: A: Publicly-available disease genome VCF
7.4 years ago by Raony Guimarães ★ 1.4k
0
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1
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8.1k
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Comment: C: NovaSeq quality analysis
7.4 years ago by Raony Guimarães ★ 1.4k
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1
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8.1k
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Comment: C: NovaSeq quality analysis
7.4 years ago by Raony Guimarães ★ 1.4k
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1
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8.1k
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Comment: C: NovaSeq quality analysis
7.4 years ago by Raony Guimarães ★ 1.4k
3
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3.6k
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Answer: A: Public Disease Exomes (VCF)
7.4 years ago by Raony Guimarães ★ 1.4k
2
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1.3k
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News: Mendel,MD: A user-friendly open-source web tool for analyzing WES and WGS in the diagnosis of patients with Mendelian disorders
variant-prioritization mendelian-disorders
updated 18 months ago by 44k • written 7.5 years ago by ★ 1.4k
3
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Answer: A: What are popular machine learning libraries/tools for Bioinformatics?
7.5 years ago by Raony Guimarães ★ 1.4k
2
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1
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9.9k
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Comment: C: [BioPython] Parse blast tabular output
7.5 years ago by Raony Guimarães ★ 1.4k
0
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1
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1.8k
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Comment: C: Different results between local and online BLAST (RefSeq database)
7.5 years ago by Raony Guimarães ★ 1.4k
2
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1
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4.6k
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Answer: A: Need some clarifications in snpEFF annotation in extracting exonic variants
8.4 years ago by Raony Guimarães ★ 1.4k
0
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0
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3.4k
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Answer: A: Mismatch in exome capture and mapping reference assembly in TCGA WXS data ?
8.4 years ago by Raony Guimarães ★ 1.4k
2
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1
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2.9k
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Answer: A: How many samples are there in 1000 genome project VCF file?
8.4 years ago by Raony Guimarães ★ 1.4k
0
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0
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1.8k
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Answer: A: which file is human gene fasta for python programming?
8.5 years ago by Raony Guimarães ★ 1.4k
0
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1
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2.3k
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Comment: C: Bioinformatics National Certification Examination (BINC)
8.5 years ago by Raony Guimarães ★ 1.4k
2
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0
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2.3k
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Answer: Answer: genome browser with genomic coordinate
updated 23 months ago by 44k • written 9.4 years ago by ★ 1.4k
0
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1
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3.1k
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Comment: Comment: ordered genome ?
updated 22 months ago by 44k • written 9.5 years ago by ★ 1.4k
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Comment: C: Alternatives to LifeScope for realigning SOLiD BAM files
9.6 years ago by Raony Guimarães ★ 1.4k
0
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1
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4.0k
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Comment: C: Alternatives to LifeScope for realigning SOLiD BAM files
9.6 years ago by Raony Guimarães ★ 1.4k
0
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0
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3.4k
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Comment: Comment: How To Force Output Strandbias In Gatk Unifiedgenotyper ?
updated 2.9 years ago by 44k • written 10.2 years ago by ★ 1.4k
2
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1
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3.9k
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Answer: Answer: miRDeep on Bio Linux
updated 3.0 years ago by 44k • written 10.3 years ago by ★ 1.4k
1
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0
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4.1k
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Answer: Answer: Dissecting number of forward/reverse reads from GATK output
updated 3.0 years ago by 44k • written 10.3 years ago by ★ 1.4k
0
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0
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Comment: C: How to generate an index (unique_key) for each genotype in a VCF File?
10.5 years ago by Raony Guimarães ★ 1.4k
0
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1
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3.7k
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Comment: C: How to generate an index (unique_key) for each genotype in a VCF File?
10.5 years ago by Raony Guimarães ★ 1.4k
0
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4
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3.7k
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How to generate an index (unique_key) for each genotype in a VCF File?
index unique_key vcf unique_id
updated 3.1 years ago by 44k • written 10.5 years ago by ★ 1.4k
1
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1
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9.2k
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Answer: A: How To Filter Vcf By Coverage?
10.7 years ago by Raony Guimarães ★ 1.4k
3
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2
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20k
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Answer: A: How To Convert .Ped To .Vcf File
11.4 years ago by Raony Guimarães ★ 1.4k
3
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0
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2.0k
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Answer: A: How Important Is It To Gather New Controls For Whole Genome And Exome Variant St
11.4 years ago by Raony Guimarães ★ 1.4k
1
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1
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2.8k
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Answer: A: Is Gatk'S Somatic Indel Detector In A Galaxy Tool Somewhere?
11.4 years ago by Raony Guimarães ★ 1.4k
0
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0
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14k
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Comment: C: Extract Coverage Track From Bam To Bed File
11.4 years ago by Raony Guimarães ★ 1.4k
0
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0
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3.5k
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Comment: C: Rnaseq: Read Length Different From Expected
11.4 years ago by Raony Guimarães ★ 1.4k
1
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1
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4.0k
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Comment: C: Realignertargetcreator Error: Not Enough Memory
11.4 years ago by Raony Guimarães ★ 1.4k
1
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0
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9.8k
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Comment: C: Is It Nonsense To Have Sift/Polyphen2 Scores For Nonsense Variants ?
11.6 years ago by Raony Guimarães ★ 1.4k
1
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1
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9.8k
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Comment: C: Is It Nonsense To Have Sift/Polyphen2 Scores For Nonsense Variants ?
11.6 years ago by Raony Guimarães ★ 1.4k
1
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1
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9.8k
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Comment: C: Is It Nonsense To Have Sift/Polyphen2 Scores For Nonsense Variants ?
11.6 years ago by Raony Guimarães ★ 1.4k
8
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6
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9.8k
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Is It Nonsense To Have Sift/Polyphen2 Scores For Nonsense Variants ?
exome variant annovar
11.6 years ago by Raony Guimarães ★ 1.4k
2
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1
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3.0k
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Answer: A: Does Anyone Know About A Biopython Package For Use With The Chado Db Schema?
11.8 years ago by Raony Guimarães ★ 1.4k
4
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0
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9.4k
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Answer: A: How To Map The Fastq With Paired-End Seq Combined In One File
updated 11.9 years ago by 101k • written 11.9 years ago by ★ 1.4k
5
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0
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10k
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Answer: A: Machine Learning Tutorials In Python
11.9 years ago by Raony Guimarães ★ 1.4k
3
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0
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19k
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Answer: A: Markduplicates: Value Was Put Into Pairinfomap More Than Once
11.9 years ago by Raony Guimarães ★ 1.4k
0
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1
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2.9k
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Comment: Comment: 1000Genome Project To Cover Gc-Rich Region?
updated 3.6 years ago by 44k • written 12.0 years ago by ★ 1.4k
0
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1
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6.0k
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Answer: A: Puzzling Error Message While Working Through A Bioconductor Tutorial On Microarr
12.1 years ago by Raony Guimarães ★ 1.4k
0
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1
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6.0k
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Comment: C: Puzzling Error Message While Working Through A Bioconductor Tutorial On Microarr
12.1 years ago by Raony Guimarães ★ 1.4k
2
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2
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2.4k
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Annotation Of Strs Using Ucsc Tables
annotation
updated 12.5 years ago by 11k • written 12.5 years ago by ★ 1.4k
0
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0
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31k
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Answer: Answer: Extract Alignment From Very Large Bam File
updated 10 months ago by 44k • written 12.5 years ago by ★ 1.4k
106 results • Page 2 of 3
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