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Comment: C: Find Intersections Between ClinVar Track and VCF In IGV
5.8 years ago by rbagnall ★ 1.8k
3
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2.9k
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Answer: A: Find Intersections Between ClinVar Track and VCF In IGV
5.8 years ago by rbagnall ★ 1.8k
3
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0
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2.3k
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Comment: C: Update RefSeq database with Ensembl VEP
5.9 years ago by rbagnall ★ 1.8k
5
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2
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2.3k
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Update RefSeq database with Ensembl VEP
Ensembl VEP Refseq
updated 5.9 years ago by 23k • written 5.9 years ago by ★ 1.8k
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Comment: C: How can I deal with this publication issue?
6.0 years ago by rbagnall ★ 1.8k
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2.5k
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Answer: A: gnomad_AF from VEP is NA
6.0 years ago by rbagnall ★ 1.8k
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Comment: C: snpEff inappropriate interpretation of variants?
6.7 years ago by rbagnall ★ 1.8k
3
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2
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5.0k
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Answer: A: snpEff inappropriate interpretation of variants?
6.7 years ago by rbagnall ★ 1.8k
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0
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2.7k
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Answer: A: Which tool to calculate per site stats on vcf file?
6.7 years ago by rbagnall ★ 1.8k
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0
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1.9k
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Answer: A: Extracting Codons from a SNP alignment
6.8 years ago by rbagnall ★ 1.8k
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1
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2.3k
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Answer: A: CNVnator error :Can't determine length for 'chr1'. No reference genome specified
6.8 years ago by rbagnall ★ 1.8k
1
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0
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2.9k
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Answer: A: Human Mitochondrial Variants Annotation
7.0 years ago by rbagnall ★ 1.8k
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0
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1.6k
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Answer: A: Do People Import VCF Files Into Databases? (2016 version)
7.6 years ago by rbagnall ★ 1.8k
0
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0
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1.2k
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Answer: A: Finding variations in mitochondrial genomes
7.7 years ago by rbagnall ★ 1.8k
6
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2
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53k
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Comment: C: How to extract specific chromosome from vcf file
7.8 years ago by rbagnall ★ 1.8k
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0
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1.5k
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Comment: C: Number of SNPs captured by targeted sequencing panels
7.9 years ago by rbagnall ★ 1.8k
1
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1.5k
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Answer: Answer: Number of SNPs captured by targeted sequencing panels
updated 12 months ago by 43k • written 7.9 years ago by ★ 1.8k
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0
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1.4k
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Answer: A: How to retrieve SNP numbers from the VCF then find information about them whethe
8.0 years ago by rbagnall ★ 1.8k
1
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1
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2.0k
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Answer: A: Targeted capture sequencing data
8.0 years ago by rbagnall ★ 1.8k
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1.4k
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Answer: A: Dataset for NGS
8.0 years ago by rbagnall ★ 1.8k
1
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0
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1.8k
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Answer: A: Can a dsRNA get sequenced on illumina with the 125bp pair end library meant for
8.1 years ago by rbagnall ★ 1.8k
1
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1
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1.6k
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Answer: A: sequence head change!
8.1 years ago by rbagnall ★ 1.8k
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1
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4.4k
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Comment: C: Using VCFTools (v0.1.13) with ExAC (release 0.3.1)
8.1 years ago by rbagnall ★ 1.8k
4
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1
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1.8k
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Answer: A: Confusing HGVS notation
8.1 years ago by rbagnall ★ 1.8k
5
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1
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6.0k
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Answer: A: Explain bioinformatics to a 10 year old
8.1 years ago by rbagnall ★ 1.8k
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1
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6.5k
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Comment: C: From gene symbol list to their coordinates
8.1 years ago by rbagnall ★ 1.8k
0
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1
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6.5k
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Answer: A: From gene symbol list to their coordinates
8.1 years ago by rbagnall ★ 1.8k
4
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1
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7.3k
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Answer: Answer: (SIFT, Polyphen, PROVEAN) vs. (ANNOVAR) vs. (LOFTEE)
updated 21 months ago by 43k • written 8.2 years ago by ★ 1.8k
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4.6k
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Comment: Comment: eigensoft smartpca error "OOPS -i flag not specified at smartpca.perl line 21
updated 21 months ago by 43k • written 8.2 years ago by ★ 1.8k
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0
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2.8k
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Comment: C: How to decide how broken a gene is
8.4 years ago by rbagnall ★ 1.8k
1
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3
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3.1k
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LOD score of a single genotype
LOD-score
updated 20 months ago by 43k • written 8.4 years ago by ★ 1.8k
1
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0
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1.6k
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Answer: Answer: RealignerTargetCreator GATK alignment
updated 18 months ago by 43k • written 8.6 years ago by ★ 1.8k
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0
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3.3k
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Comment: Comment: Whole exome length of exons from bam file
updated 19 months ago by 43k • written 8.6 years ago by ★ 1.8k
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0
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8.5k
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Answer: Answer: PCA plot Fig software
updated 19 months ago by 43k • written 8.6 years ago by ★ 1.8k
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0
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4.9k
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Comment: Comment: Variant calling for MNP
updated 18 months ago by 43k • written 8.7 years ago by ★ 1.8k
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0
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4.9k
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Comment: C: Variant calling for MNP
8.7 years ago by rbagnall ★ 1.8k
0
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1
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4.9k
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Comment: Comment: Variant calling for MNP
updated 18 months ago by 43k • written 8.7 years ago by ★ 1.8k
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0
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5.9k
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Comment: Comment: vcf SNP file minor allele frequency filter?
updated 18 months ago by 43k • written 8.7 years ago by ★ 1.8k
1
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0
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18k
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Comment: Comment: Extract a particular data from text file using perl
updated 17 months ago by 43k • written 8.8 years ago by ★ 1.8k
4
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0
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2.2k
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Answer: Answer: Looking for Jewish Exoms
updated 18 months ago by 43k • written 8.8 years ago by ★ 1.8k
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2
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4.1k
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Comment: C: What's the best way to find all the possible cutting sites of an sequence-specif
8.8 years ago by rbagnall ★ 1.8k
1
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1
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5.0k
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Comment: Comment: EIGENSOFT : Ploteig, 3D Plots
updated 16 months ago by 43k • written 8.8 years ago by ★ 1.8k
5
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1
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5.0k
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Answer: Answer: EIGENSOFT : Ploteig, 3D Plots
updated 16 months ago by 43k • written 8.8 years ago by ★ 1.8k
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0
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6.8k
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Answer: A: eigenstrat smartpca input files
8.9 years ago by rbagnall ★ 1.8k
4
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2
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3.9k
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Answer: Answer: Large tab-delimited table of SNP data, how to filter out some rows based on rsID
updated 15 months ago by 43k • written 8.9 years ago by ★ 1.8k
0
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1
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2.5k
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Answer: Answer: Finding common genes
updated 15 months ago by 43k • written 8.9 years ago by ★ 1.8k
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2
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Comment: C: Is there software that takes advantage of MarkedDuplicates for SNP calling?
9.0 years ago by rbagnall ★ 1.8k
0
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0
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2.9k
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Comment: Comment: Block break from gVCF files
updated 22 months ago by 43k • written 9.1 years ago by ★ 1.8k
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0
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Comment: C: Block break from gVCF files
9.1 years ago by rbagnall ★ 1.8k
0
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1
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2.9k
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Answer: Answer: Block break from gVCF files
updated 22 months ago by 43k • written 9.1 years ago by ★ 1.8k
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