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Comment: Comment: BWA-mem not working with Snakemake + singularity
14 months ago by brunobsouzaa ▴ 830
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1.2k
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Comment: Comment: BWA-mem not working with Snakemake + singularity
15 months ago by brunobsouzaa ▴ 830
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911
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Comment: Comment: How to use a variable to install an R package
16 months ago by brunobsouzaa ▴ 830
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629
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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
19 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?
21 months ago by brunobsouzaa ▴ 830
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1.4k
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Comment: Comment: GATK's selectVariants not outputting VCF
21 months ago by brunobsouzaa ▴ 830
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1.4k
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Comment: Comment: GATK's selectVariants not outputting VCF
21 months ago by brunobsouzaa ▴ 830
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774
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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
22 months ago by brunobsouzaa ▴ 830
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1.4k
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Comment: Comment: Biopython Code to Convert DNA FASTA file to Protein FASTA file
22 months ago by brunobsouzaa ▴ 830
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1
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1.1k
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Comment: Comment: VEP synonyms file
22 months ago by brunobsouzaa ▴ 830
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867
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Comment: Comment: add VAF to VCF
22 months ago by brunobsouzaa ▴ 830
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828
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Comment: Comment: PLINK CASE-CONTROL ANALYSIS
22 months ago by brunobsouzaa ▴ 830
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437
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Comment: Comment: How can I transform a three column data frame into a binary-table in R?
23 months ago by brunobsouzaa ▴ 830
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723
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Comment: Comment: Deleting all the rows from ANY column that contain a key word
23 months ago by brunobsouzaa ▴ 830
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1
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587
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Comment: Comment: The minor allele frequency
2.0 years ago by brunobsouzaa ▴ 830
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706
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Comment: Comment: miRNAs pathway analysis
2.0 years ago by brunobsouzaa ▴ 830
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1.2k
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Comment: Comment: Detect Structural varirant from VCF file
2.0 years ago by brunobsouzaa ▴ 830
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1
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713
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Comment: Comment: Statistical methods to determine descrimimant variables between two groups
2.0 years ago by brunobsouzaa ▴ 830
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609
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Comment: Comment: gatk requests enormous amounts of memory. How to limit it?
2.0 years ago by brunobsouzaa ▴ 830
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1.4k
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Comment: Comment: Hard filtering on GATK HaplotypeCaller giving multiple warnings
2.1 years ago by brunobsouzaa ▴ 830
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861
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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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959
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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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572
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Comment: Comment: Filter track list and variant list
2.2 years ago by brunobsouzaa ▴ 830
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964
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Comment: Comment: STAR aligment generating genome index
2.2 years ago by brunobsouzaa ▴ 830
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463
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Comment: Comment: RNA-seq alignment in 2 pass mode
2.2 years ago by brunobsouzaa ▴ 830
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643
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Comment: Comment: edgeR, how to write the model matrix for comparison?
2.2 years ago by brunobsouzaa ▴ 830
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530
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Comment: Comment: Sanger sequencing
2.2 years ago by brunobsouzaa ▴ 830
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587
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Comment: Comment: How to detect CNV via readDepth with multiple samples
2.3 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
2.3 years ago by brunobsouzaa ▴ 830
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1
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1.0k
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Comment: Comment: Merging .bam files in STAR
2.3 years ago by brunobsouzaa ▴ 830
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707
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Comment: Comment: Vep combined or single
2.3 years ago by brunobsouzaa ▴ 830
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1
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707
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Comment: Comment: Vep combined or single
2.3 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
2.4 years ago by brunobsouzaa ▴ 830
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1
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853
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Comment: Comment: Adding flanking regions to a gene for primer design
2.4 years ago by brunobsouzaa ▴ 830
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944
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Comment: Comment: CNV kit merge all my gene names together
2.4 years ago by brunobsouzaa ▴ 830
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2.7k
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Comment: Comment: How to extract specific field from VCF?
2.4 years ago by brunobsouzaa ▴ 830
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640
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Comment: Comment: ANNOVAR
2.4 years ago by brunobsouzaa ▴ 830
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758
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Comment: Comment: Looking for a Bioinformatics Certification course
2.4 years ago by brunobsouzaa ▴ 830
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1.0k
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Comment: Comment: RNA seq
2.5 years ago by brunobsouzaa ▴ 830
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2
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1.0k
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Comment: Comment: RNA seq
updated 2.5 years ago by 13k • written 2.5 years ago by ▴ 830
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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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1.5k
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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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578
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Comment: Comment: Individual or joint variant call ing
2.5 years ago by brunobsouzaa ▴ 830
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808
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Comment: Comment: annotating vcf with variant type and variant effect, and most harmful effect
2.6 years ago by brunobsouzaa ▴ 830
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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?
2.6 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
2.6 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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