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1
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926
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Comment: C: Problems removing a subset of individuals from ped files
3.7 years ago by Nicolas Rosewick 11k
1
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1
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2.7k
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Comment: C: Imputation results from TOPMED server
3.8 years ago by Nicolas Rosewick 11k
1
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1
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2.7k
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Comment: C: Imputation results from TOPMED server
3.8 years ago by Nicolas Rosewick 11k
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0
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1.3k
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Comment: C: Reverse allele frequency
3.8 years ago by Nicolas Rosewick 11k
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1
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1.3k
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Comment: C: Reverse allele frequency
3.8 years ago by Nicolas Rosewick 11k
0
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1
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884
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Comment: C: Plots for gene expression data
3.8 years ago by Nicolas Rosewick 11k
2
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1
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2.6k
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Comment: C: Calculate p-value from Weibull distribution?
3.8 years ago by Nicolas Rosewick 11k
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0
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1.1k
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Comment: C: population stratification using PLINK
3.8 years ago by Nicolas Rosewick 11k
0
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1
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827
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Comment: C: Chromosome position sample files merging in R
3.8 years ago by Nicolas Rosewick 11k
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0
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736
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Comment: C: Population stratification with PLINK
3.8 years ago by Nicolas Rosewick 11k
1
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1
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692
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Comment: C: How to create MAplot in R for only one sample?
3.9 years ago by Nicolas Rosewick 11k
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0
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747
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Comment: C: Multiple hypothesis testing
3.9 years ago by Nicolas Rosewick 11k
0
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1
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3.2k
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Comment: C: PCA: log transform and scale=T/F?
3.9 years ago by Nicolas Rosewick 11k
1
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1
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920
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Comment: C: gnoMAD mutation and essential gene
4.0 years ago by Nicolas Rosewick 11k
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2
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1.0k
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Comment: C: how to find candidate genes using linear regression in R
4.0 years ago by Nicolas Rosewick 11k
0
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1
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1.0k
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Comment: C: Structural variation germline vs somatic ?
4.1 years ago by Nicolas Rosewick 11k
0
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0
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742
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Comment: C: bam file: get date that alignment was run
4.1 years ago by Nicolas Rosewick 11k
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0
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4.4k
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Comment: C: Use padj instead of p-value to ploting DE genes using EnhancedVolcano
4.1 years ago by Nicolas Rosewick 11k
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0
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2.3k
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Comment: C: [SOLVED] vcfanno: issues to annotate VCF with gnomAD r3.0
4.1 years ago by Nicolas Rosewick 11k
0
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0
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1.2k
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Comment: C: Retrieving multiple regions (from a list) in a bam file and outputing as a table
4.1 years ago by Nicolas Rosewick 11k
0
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1
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1.2k
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Comment: C: Retrieving multiple regions (from a list) in a bam file and outputing as a table
4.1 years ago by Nicolas Rosewick 11k
1
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1
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3.7k
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Comment: C: script in R to convert DNA to RNA sequence
4.2 years ago by Nicolas Rosewick 11k
0
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1
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2.8k
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Comment: C: feature selection using random forest
4.2 years ago by Nicolas Rosewick 11k
0
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0
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1.1k
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Comment: C: Cutdapt for batch processing ?
4.2 years ago by Nicolas Rosewick 11k
0
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1
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4.4k
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Comment: C: GSVA on RNAseq data (GTEX)
4.2 years ago by Nicolas Rosewick 11k
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0
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1.2k
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Comment: C: Scatter / Gather for BaseRecalibrator on a single human WES dataset?
4.2 years ago by Nicolas Rosewick 11k
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1
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2.7k
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Comment: C: Should I keep up with random contigs in human genome
4.3 years ago by Nicolas Rosewick 11k
2
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0
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2.1k
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Comment: C: Remove duplicate reads before variant calling?
4.3 years ago by Nicolas Rosewick 11k
1
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0
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1.6k
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Comment: C: Should I merge the Paired-end RNA-seq reads for BLAT for intron identification
4.3 years ago by Nicolas Rosewick 11k
0
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1
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2.3k
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Comment: C: Student's t-test (For Paired samples) calculation
updated 4.3 years ago by 43k • written 8.2 years ago by 11k
0
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1
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4.4k
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Comment: C: What causes tophat_reports error?
updated 4.3 years ago by 43k • written 9.9 years ago by 11k
0
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0
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2.6k
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Comment: C: samtools + map
updated 4.4 years ago by 43k • written 10.0 years ago by 11k
0
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0
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7.2k
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Comment: C: Pick random position from specific genomic regions
updated 4.4 years ago by 43k • written 10.1 years ago by 11k
0
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0
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7.2k
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Comment: C: Pick random position from specific genomic regions
updated 4.4 years ago by 43k • written 10.1 years ago by 11k
0
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1
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7.2k
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Comment: C: Pick random position from specific genomic regions
updated 4.4 years ago by 43k • written 10.1 years ago by 11k
0
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1
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1.1k
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Comment: C: Homozygot genotype information but SNP is heterozygous
4.4 years ago by Nicolas Rosewick 11k
2
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1
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6.9k
views
Comment: C: How to TMM after HTSeq-count?
updated 4.4 years ago by 43k • written 8.4 years ago by 11k
0
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1
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740
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Comment: C: Overlap two variable
4.4 years ago by Nicolas Rosewick 11k
0
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0
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727
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Comment: C: grouping of maf results in GWAS
4.4 years ago by Nicolas Rosewick 11k
0
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0
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8.7k
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Comment: C: Bwa Specify Number Of Maximum Mismatches And Gaps
updated 4.4 years ago by 43k • written 12.5 years ago by 11k
0
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0
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3.4k
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Comment: C: The best aligner to align RNA-Seq data into mitochondria genome
updated 4.4 years ago by 43k • written 8.4 years ago by 11k
0
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1
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1.0k
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Comment: C: GWAS result too significant
4.4 years ago by Nicolas Rosewick 11k
0
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1
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1.6k
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Comment: C: Germline - somatic mutation co-occurrence analysis
4.4 years ago by Nicolas Rosewick 11k
0
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1
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1.6k
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Comment: C: Germline - somatic mutation co-occurrence analysis
4.4 years ago by Nicolas Rosewick 11k
0
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0
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3.8k
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Comment: C: deseq2 read counts vs featurecount read counts
4.5 years ago by Nicolas Rosewick 11k
1
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1
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3.8k
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Comment: C: deseq2 read counts vs featurecount read counts
4.5 years ago by Nicolas Rosewick 11k
1
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0
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2.0k
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Comment: C: using DEseq to produce RPKM and VST
updated 4.5 years ago by 43k • written 8.6 years ago by 11k
1
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0
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1.4k
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Comment: C: Run R script on 100 files using for loop
4.5 years ago by Nicolas Rosewick 11k
2
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0
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1.2k
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Comment: C: Fisher's exact test for Copy Number Variation association in R
4.5 years ago by Nicolas Rosewick 11k
0
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1
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5.8k
views
Comment: C: GATK quality recalibration to get recalibrated BAM files before SNP calling
4.5 years ago by Nicolas Rosewick 11k
637 results • Page 2 of 13
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