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Comment: Comment: User friendly (visual&interactive) VCF/BCF mining tools (2021)
2.7 years ago by desouzareis.r ▴ 280
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Comment: Comment: User friendly (visual&interactive) VCF/BCF mining tools (2021)
2.7 years ago by desouzareis.r ▴ 280
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1.1k
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Comment: Comment: Annotate Structural variants with population specific allele frequency values
2.7 years ago by desouzareis.r ▴ 280
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Comment: Comment: How does one harmonize WGS data with Microarray data?
2.7 years ago by desouzareis.r ▴ 280
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Comment: Comment: GIAB Benchmark (High Confidence) Bed Filles
2.7 years ago by desouzareis.r ▴ 280
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2
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1.5k
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Comment: Comment: GIAB Benchmark (High Confidence) Bed Filles
2.7 years ago by desouzareis.r ▴ 280
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676
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Comment: Comment: Precision of variant calling (INDELs)
3.1 years ago by desouzareis.r ▴ 280
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1.4k
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Comment: Comment: GATK no "SB" annotation after GenotypeGVCFs
3.1 years ago by desouzareis.r ▴ 280
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1.3k
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Comment: Comment: A simple question about UCSC genome browser
3.2 years ago by desouzareis.r ▴ 280
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994
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Comment: Comment: search of genomic annotation databases
3.2 years ago by desouzareis.r ▴ 280
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629
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Comment: Comment: Question about the DbSNP reference vcfs
3.2 years ago by desouzareis.r ▴ 280
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1.5k
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Comment: Comment: Selecting genotypes for a specific chromosome belonging to a specific patient fr
3.2 years ago by desouzareis.r ▴ 280
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707
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Comment: C: Deletions together with SNVs on BAM files
3.2 years ago by desouzareis.r ▴ 280
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1
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1.1k
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Comment: C: Lengths of UTR3, UTR5 and ORF from gtf file
3.2 years ago by desouzareis.r ▴ 280
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776
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Comment: C: Discrepancy between Genome Browser hg19 phyloP Score and that of wig data
3.2 years ago by desouzareis.r ▴ 280
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1
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793
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Comment: C: How to make paired-end sequencing multi-mapping reads have only the optimal two
3.2 years ago by desouzareis.r ▴ 280
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1
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2.2k
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Comment: C: IDT xGen Exome Research Panel v2 vs Twist Human exome core
3.2 years ago by desouzareis.r ▴ 280
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956
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Comment: C: Cheat Sheet for NGS data analysis
3.2 years ago by desouzareis.r ▴ 280
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1
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5.8k
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Comment: C: How to keep only Biallelic SNP in vcf
3.2 years ago by desouzareis.r ▴ 280
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1
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5.8k
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Comment: C: How to keep only Biallelic SNP in vcf
3.2 years ago by desouzareis.r ▴ 280
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2.9k
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Comment: C: How to convert plink data from 38th assembly to 37
3.2 years ago by desouzareis.r ▴ 280
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1
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740
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Comment: C: refGene Python Api
3.2 years ago by desouzareis.r ▴ 280
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665
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Comment: C: how to get the best alignment from the sam file
3.2 years ago by desouzareis.r ▴ 280
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1.8k
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Comment: C: Generate consensus from contig alignment to reference sequence
3.2 years ago by desouzareis.r ▴ 280
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1.3k
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Comment: C: Difference between read depth, allelic depth and bam readcounts
3.2 years ago by desouzareis.r ▴ 280
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2.0k
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Comment: C: Effect of removing secondary/supplementary alignments from BAM file?
3.2 years ago by desouzareis.r ▴ 280
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2
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967
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Comment: C: extract region.txt from bam file
3.2 years ago by desouzareis.r ▴ 280
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1
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982
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Comment: C: chr20_KI270871v1_alt in HG38 Broad Variant and Blacklist regions
3.2 years ago by desouzareis.r ▴ 280
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1
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1.0k
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Comment: C: qiaseq panel fastq to vcf
3.2 years ago by desouzareis.r ▴ 280
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2
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1.0k
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Comment: C: qiaseq panel fastq to vcf
3.2 years ago by desouzareis.r ▴ 280
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0
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470
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Comment: C: How will the fusion sequence looks like in RNA level
3.2 years ago by desouzareis.r ▴ 280
1
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1
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691
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Comment: C: Minimum overlap when comparing BED files
3.2 years ago by desouzareis.r ▴ 280
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705
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Comment: C: Query regarding variant calling and reporting
3.2 years ago by desouzareis.r ▴ 280
1
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0
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899
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Comment: C: Data access through python
3.2 years ago by desouzareis.r ▴ 280
1
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779
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Comment: C: how to determine low quality variants in vcf files
3.2 years ago by desouzareis.r ▴ 280
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1
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705
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Comment: C: Query regarding variant calling and reporting
3.2 years ago by desouzareis.r ▴ 280
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473
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Comment: C: tool for visualizing small sets of genes
3.2 years ago by desouzareis.r ▴ 280
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680
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Comment: C: Common SNPs (UCSC genome browser)
3.2 years ago by desouzareis.r ▴ 280
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0
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3.0k
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Comment: C: Is there any method to convert a text file to VCF format?
3.2 years ago by desouzareis.r ▴ 280
1
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11k
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Comment: C: Correct way to calculate VAF (Variant allele fraction) from a VCF file
3.2 years ago by desouzareis.r ▴ 280
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0
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987
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Comment: C: fastqc report and quality check
3.2 years ago by desouzareis.r ▴ 280
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0
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972
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Comment: C: which tool should be used to call the genotype?
3.2 years ago by desouzareis.r ▴ 280
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1.6k
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Comment: C: Converting Bigwiggle (.bw) to bed
3.3 years ago by desouzareis.r ▴ 280
1
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2.1k
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Comment: C: Append characters to end of fasta sequences in a multifasta file
3.3 years ago by desouzareis.r ▴ 280
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0
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1.7k
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Comment: C: Convert processed bam file to fastq
3.3 years ago by desouzareis.r ▴ 280
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0
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1.0k
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Comment: C: Splitting info field in Annovar's multianno.txt file
3.3 years ago by desouzareis.r ▴ 280
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0
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6.4k
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Comment: C: Samtools bam2fq converting bam file to fastq. What happens to unmapped reads?
3.3 years ago by desouzareis.r ▴ 280
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