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Comment: Comment: BWA-mem not working with Snakemake + singularity
13 months ago by brunobsouzaa ▴ 830
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1.2k
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Comment: Comment: BWA-mem not working with Snakemake + singularity
14 months ago by brunobsouzaa ▴ 830
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897
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Comment: Comment: How to use a variable to install an R package
15 months ago by brunobsouzaa ▴ 830
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613
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Comment: Comment: Bioinformatics analysis from raw data to disease driver variants
18 months ago by brunobsouzaa ▴ 830
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2.1k
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Comment: Comment: Germline variant calling pipeline using Snakemake
18 months ago by brunobsouzaa ▴ 830
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1.2k
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Comment: Comment: How DESeq2 formula correction works?
20 months ago by brunobsouzaa ▴ 830
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1.3k
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Comment: Comment: Is there a way to convert a .vcf.gz.tbi file back to a .vcf.gz or .vcf file?
20 months ago by brunobsouzaa ▴ 830
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1.4k
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Comment: Comment: GATK's selectVariants not outputting VCF
20 months ago by brunobsouzaa ▴ 830
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1.4k
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Comment: Comment: GATK's selectVariants not outputting VCF
20 months ago by brunobsouzaa ▴ 830
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757
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Comment: Comment: Illumina base space
21 months ago by brunobsouzaa ▴ 830
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1.7k
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Comment: Comment: Count regions that overlap with python
21 months ago by brunobsouzaa ▴ 830
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1.3k
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Comment: Comment: Biopython Code to Convert DNA FASTA file to Protein FASTA file
21 months ago by brunobsouzaa ▴ 830
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1
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1.0k
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Comment: Comment: VEP synonyms file
21 months ago by brunobsouzaa ▴ 830
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844
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Comment: Comment: add VAF to VCF
21 months ago by brunobsouzaa ▴ 830
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1
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807
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Comment: Comment: PLINK CASE-CONTROL ANALYSIS
22 months ago by brunobsouzaa ▴ 830
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422
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Comment: Comment: How can I transform a three column data frame into a binary-table in R?
22 months ago by brunobsouzaa ▴ 830
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706
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Comment: Comment: Deleting all the rows from ANY column that contain a key word
22 months ago by brunobsouzaa ▴ 830
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1
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578
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Comment: Comment: The minor allele frequency
23 months ago by brunobsouzaa ▴ 830
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692
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Comment: Comment: miRNAs pathway analysis
23 months ago by brunobsouzaa ▴ 830
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1.1k
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Comment: Comment: Detect Structural varirant from VCF file
23 months ago by brunobsouzaa ▴ 830
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1
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689
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Comment: Comment: Statistical methods to determine descrimimant variables between two groups
23 months ago by brunobsouzaa ▴ 830
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597
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Comment: Comment: gatk requests enormous amounts of memory. How to limit it?
23 months ago by brunobsouzaa ▴ 830
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1.3k
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Comment: Comment: Hard filtering on GATK HaplotypeCaller giving multiple warnings
2.0 years ago by brunobsouzaa ▴ 830
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839
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Comment: Comment: remove vcf variants from bam
2.1 years ago by brunobsouzaa ▴ 830
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1
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936
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Comment: Comment: for loop with basename created one merged sam file instead of multiple separate
2.1 years ago by brunobsouzaa ▴ 830
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561
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Comment: Comment: Filter track list and variant list
2.1 years ago by brunobsouzaa ▴ 830
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1
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899
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Comment: Comment: STAR aligment generating genome index
2.1 years ago by brunobsouzaa ▴ 830
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456
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Comment: Comment: RNA-seq alignment in 2 pass mode
2.1 years ago by brunobsouzaa ▴ 830
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1
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628
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Comment: Comment: edgeR, how to write the model matrix for comparison?
2.1 years ago by brunobsouzaa ▴ 830
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517
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Comment: Comment: Sanger sequencing
2.2 years ago by brunobsouzaa ▴ 830
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576
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Comment: Comment: How to detect CNV via readDepth with multiple samples
2.2 years ago by brunobsouzaa ▴ 830
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2.3k
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Comment: Comment: How to split text into columns using R
2.2 years ago by brunobsouzaa ▴ 830
1
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1
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981
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Comment: Comment: Merging .bam files in STAR
2.2 years ago by brunobsouzaa ▴ 830
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691
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Comment: Comment: Vep combined or single
2.2 years ago by brunobsouzaa ▴ 830
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1
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691
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Comment: Comment: Vep combined or single
2.2 years ago by brunobsouzaa ▴ 830
0
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0
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1.4k
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Comment: Comment: Snakemake issue
2.3 years ago by brunobsouzaa ▴ 830
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1
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823
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Comment: Comment: Adding flanking regions to a gene for primer design
2.3 years ago by brunobsouzaa ▴ 830
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925
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Comment: Comment: CNV kit merge all my gene names together
2.3 years ago by brunobsouzaa ▴ 830
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2.6k
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Comment: Comment: How to extract specific field from VCF?
2.3 years ago by brunobsouzaa ▴ 830
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629
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Comment: Comment: ANNOVAR
2.3 years ago by brunobsouzaa ▴ 830
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746
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Comment: Comment: Looking for a Bioinformatics Certification course
2.4 years ago by brunobsouzaa ▴ 830
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0
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983
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Comment: Comment: RNA seq
2.4 years ago by brunobsouzaa ▴ 830
1
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2
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983
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Comment: Comment: RNA seq
updated 2.4 years ago by 13k • written 2.4 years ago by ▴ 830
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1
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1.2k
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Comment: Comment: ApplyBQSR won't recognise output argument
2.5 years ago by brunobsouzaa ▴ 830
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1.4k
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Comment: Comment: Calculatio median in a Fastq file using bioawk/awk
2.5 years ago by brunobsouzaa ▴ 830
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566
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Comment: Comment: Individual or joint variant call ing
2.5 years ago by brunobsouzaa ▴ 830
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801
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Comment: Comment: annotating vcf with variant type and variant effect, and most harmful effect
2.5 years ago by brunobsouzaa ▴ 830
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0
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1.0k
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Comment: Comment: Is it possible to detect CNV without having a reference control group/sample?
2.5 years ago by brunobsouzaa ▴ 830
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1
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2.3k
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Comment: Comment: How we can put PASS filters on all variants in your VCF file and create a separ
2.5 years ago by brunobsouzaa ▴ 830
1
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0
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1.5k
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Comment: Comment: DESeq2 error in design~ code
2.6 years ago by brunobsouzaa ▴ 830
174 results • Page 1 of 4
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