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Comment: Comment: User friendly (visual&interactive) VCF/BCF mining tools (2021)
4.1 years ago by desouzareis.r ▴ 290
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5.8k
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Comment: Comment: User friendly (visual&interactive) VCF/BCF mining tools (2021)
4.1 years ago by desouzareis.r ▴ 290
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1.8k
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Comment: Comment: Annotate Structural variants with population specific allele frequency values
4.2 years ago by desouzareis.r ▴ 290
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2.2k
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Comment: Comment: How does one harmonize WGS data with Microarray data?
4.2 years ago by desouzareis.r ▴ 290
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2.5k
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Comment: Comment: GIAB Benchmark (High Confidence) Bed Filles
4.2 years ago by desouzareis.r ▴ 290
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2.5k
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Comment: Comment: GIAB Benchmark (High Confidence) Bed Filles
4.2 years ago by desouzareis.r ▴ 290
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1.0k
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Comment: Comment: Precision of variant calling (INDELs)
4.6 years ago by desouzareis.r ▴ 290
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1.8k
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Comment: Comment: GATK no "SB" annotation after GenotypeGVCFs
4.6 years ago by desouzareis.r ▴ 290
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Comment: Comment: A simple question about UCSC genome browser
4.6 years ago by desouzareis.r ▴ 290
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1.4k
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Answer: Answer: ANNOVAR doesn't recognize multiple variants at single locus
4.6 years ago by desouzareis.r ▴ 290
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18k
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Answer: Answer: Is Human_G1K_V37.Fasta Hg19?
4.6 years ago by desouzareis.r ▴ 290
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1.1k
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Answer: Comment: genotype matrix
4.6 years ago by desouzareis.r ▴ 290
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2.2k
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Answer: Comment: What is the difference between breakends and breakpoints?
4.6 years ago by desouzareis.r ▴ 290
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1.4k
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Comment: Comment: search of genomic annotation databases
4.6 years ago by desouzareis.r ▴ 290
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917
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Comment: Comment: Question about the DbSNP reference vcfs
4.6 years ago by desouzareis.r ▴ 290
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2.0k
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Comment: Comment: Selecting genotypes for a specific chromosome belonging to a specific patient fr
4.6 years ago by desouzareis.r ▴ 290
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2
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2.0k
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Answer: Comment: Selecting genotypes for a specific chromosome belonging to a specific patient fr
4.6 years ago by desouzareis.r ▴ 290
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1.0k
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Comment: C: Deletions together with SNVs on BAM files
4.6 years ago by desouzareis.r ▴ 290
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1
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1.6k
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Comment: C: Lengths of UTR3, UTR5 and ORF from gtf file
4.6 years ago by desouzareis.r ▴ 290
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1
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1.2k
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Comment: C: Discrepancy between Genome Browser hg19 phyloP Score and that of wig data
4.6 years ago by desouzareis.r ▴ 290
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1
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1.2k
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Comment: C: How to make paired-end sequencing multi-mapping reads have only the optimal two
4.6 years ago by desouzareis.r ▴ 290
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1
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3.1k
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Comment: C: IDT xGen Exome Research Panel v2 vs Twist Human exome core
4.6 years ago by desouzareis.r ▴ 290
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1.3k
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Comment: C: Cheat Sheet for NGS data analysis
4.6 years ago by desouzareis.r ▴ 290
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1
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9.1k
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Comment: C: How to keep only Biallelic SNP in vcf
4.6 years ago by desouzareis.r ▴ 290
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1
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9.1k
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Comment: C: How to keep only Biallelic SNP in vcf
4.6 years ago by desouzareis.r ▴ 290
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0
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4.1k
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Comment: C: How to convert plink data from 38th assembly to 37
4.6 years ago by desouzareis.r ▴ 290
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1
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1.5k
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Comment: C: refGene Python Api
4.6 years ago by desouzareis.r ▴ 290
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928
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Comment: C: how to get the best alignment from the sam file
4.6 years ago by desouzareis.r ▴ 290
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2.3k
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Comment: C: Generate consensus from contig alignment to reference sequence
4.6 years ago by desouzareis.r ▴ 290
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2.0k
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Comment: C: Difference between read depth, allelic depth and bam readcounts
4.6 years ago by desouzareis.r ▴ 290
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3.0k
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Comment: C: Effect of removing secondary/supplementary alignments from BAM file?
4.6 years ago by desouzareis.r ▴ 290
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1
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3.0k
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Answer: C: Effect of removing secondary/supplementary alignments from BAM file?
4.6 years ago by desouzareis.r ▴ 290
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2
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1.5k
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Comment: C: extract region.txt from bam file
4.6 years ago by desouzareis.r ▴ 290
3
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1
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4.5k
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Answer: A: Can't create tabix index of the bed file
4.6 years ago by desouzareis.r ▴ 290
1
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1
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1.4k
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Comment: C: chr20_KI270871v1_alt in HG38 Broad Variant and Blacklist regions
4.6 years ago by desouzareis.r ▴ 290
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1.6k
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Comment: C: qiaseq panel fastq to vcf
4.6 years ago by desouzareis.r ▴ 290
1
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2
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1.6k
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Comment: C: qiaseq panel fastq to vcf
4.7 years ago by desouzareis.r ▴ 290
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0
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731
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Comment: C: How will the fusion sequence looks like in RNA level
4.7 years ago by desouzareis.r ▴ 290
1
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1
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1.2k
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Comment: C: Minimum overlap when comparing BED files
4.7 years ago by desouzareis.r ▴ 290
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0
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1.2k
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Comment: C: Query regarding variant calling and reporting
4.7 years ago by desouzareis.r ▴ 290
1
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0
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1.3k
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Comment: C: Data access through python
4.7 years ago by desouzareis.r ▴ 290
1
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0
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1.1k
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Comment: C: how to determine low quality variants in vcf files
4.7 years ago by desouzareis.r ▴ 290
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1
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1.2k
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Comment: C: Query regarding variant calling and reporting
4.7 years ago by desouzareis.r ▴ 290
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0
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744
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Comment: C: tool for visualizing small sets of genes
4.7 years ago by desouzareis.r ▴ 290
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0
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1.0k
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Comment: C: Common SNPs (UCSC genome browser)
4.7 years ago by desouzareis.r ▴ 290
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5.0k
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Comment: C: Is there any method to convert a text file to VCF format?
4.7 years ago by desouzareis.r ▴ 290
2
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1
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15k
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Comment: C: Correct way to calculate VAF (Variant allele fraction) from a VCF file
4.7 years ago by desouzareis.r ▴ 290
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0
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1.7k
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Comment: C: fastqc report and quality check
4.7 years ago by desouzareis.r ▴ 290
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0
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1.3k
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Comment: C: which tool should be used to call the genotype?
4.7 years ago by desouzareis.r ▴ 290
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0
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2.1k
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Comment: C: Converting Bigwiggle (.bw) to bed
4.7 years ago by desouzareis.r ▴ 290
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