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3
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1.0k
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Answer: A: @RG ( read group ) in neandertals
updated 4.7 years ago by 82k • written 4.7 years ago by 47k
1
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0
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1.5k
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Answer: A: Assembly and read comparison using kmers
4.7 years ago by WouterDeCoster 47k
3
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1.8k
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Answer: A: N 50 Value
4.7 years ago by WouterDeCoster 47k
4
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1
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3.1k
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Answer: A: Oxford Nanopore sequencing_summary.txt file description
4.7 years ago by WouterDeCoster 47k
5
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1
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1.1k
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Answer: C: gene transcription direction
4.7 years ago by WouterDeCoster 47k
5
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1
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2.9k
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Answer: A: Converting and sorting .sam at the same time
4.7 years ago by WouterDeCoster 47k
1
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0
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820
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Answer: A: How can I assess the probability of a gene being disease-related?
4.7 years ago by WouterDeCoster 47k
3
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1
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2.1k
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Answer: A: Gene co-expression network construction
4.7 years ago by WouterDeCoster 47k
2
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1
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1.3k
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Answer: A: RNA-Seq Differential gene expression
4.7 years ago by WouterDeCoster 47k
1
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0
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879
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Answer: A: Strand information for reference genome
4.7 years ago by WouterDeCoster 47k
1
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2
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5.3k
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Answer: A: How to trim poly-sequence before or after trimming by Trimmomatic.
4.7 years ago by WouterDeCoster 47k
1
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1
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934
views
Answer: A: Any paternity testing tutorial?
4.7 years ago by WouterDeCoster 47k
1
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1
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15k
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Answer: A: Where to download MinKnow software of MinION from?
4.7 years ago by WouterDeCoster 47k
3
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2
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6.7k
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Answer: A: Using Graphics Processing Units (GPUs) in bioinformatics
4.7 years ago by WouterDeCoster 47k
1
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1
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1.1k
views
Answer: A: Comparing two cnv call files?
4.7 years ago by WouterDeCoster 47k
0
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0
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2.6k
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Answer: A: Using rmats on bioconda
4.8 years ago by WouterDeCoster 47k
2
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0
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1.7k
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Answer: A: featureCount Too Many Genes
4.8 years ago by WouterDeCoster 47k
0
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1
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1.4k
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Answer: A: Ideas on how to evaluate genomic coordinates remapping tools?
4.8 years ago by WouterDeCoster 47k
0
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1
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1.5k
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Answer: C: Location of centromere
4.8 years ago by WouterDeCoster 47k
1
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1
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1.2k
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Answer: A: comparing kallisto rsem , makind sd plot and corelation table /graph
4.8 years ago by WouterDeCoster 47k
4
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0
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1.2k
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Answer: C: Doing differential gene expression without knowing sample classes
4.8 years ago by WouterDeCoster 47k
1
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1
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945
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Answer: A: A small detail when use VEP
4.8 years ago by WouterDeCoster 47k
6
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1
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4.5k
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Answer: A: How to use htseq-count with several samples ?
4.9 years ago by WouterDeCoster 47k
5
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1
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3.3k
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Answer: A: What is "mappability"?
4.9 years ago by WouterDeCoster 47k
2
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2
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8.3k
views
Answer: A: samtools sort: failed to create temporary file "/BOredq/NA12878.sorted.bam.tmp.0
4.9 years ago by WouterDeCoster 47k
5
votes
2
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11k
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Answer: A: Proceccing Raw Nanopore Data
4.9 years ago by WouterDeCoster 47k
1
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0
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2.0k
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Answer: A: Confused about TSS coordinates
4.9 years ago by WouterDeCoster 47k
2
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1
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3.2k
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Answer: A: peaks in IGV
4.9 years ago by WouterDeCoster 47k
2
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2
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9.3k
views
Answer: A: Nanopore data and downstream anlysis
4.9 years ago by WouterDeCoster 47k
1
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0
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2.0k
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Answer: A: Export Coverage on IGV
4.9 years ago by WouterDeCoster 47k
1
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1
reply
2.3k
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Answer: A: Illumina hiseq 2500 strand specificity for paired-end datasets
4.9 years ago by WouterDeCoster 47k
3
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1
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3.3k
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Answer: A: Can you detect novel (non-coding) transcripts using Salmon and the hg38 transcri
4.9 years ago by WouterDeCoster 47k
3
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1
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1.1k
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Answer: C: Are small insertions always single-stranded?
4.9 years ago by WouterDeCoster 47k
3
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1
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1.8k
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Answer: A: How to predict sample ethnicty from a VCF using 1000G or gnomAD ?
4.9 years ago by WouterDeCoster 47k
1
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1
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908
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Answer: C: select of genes
4.9 years ago by WouterDeCoster 47k
1
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1
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1.0k
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Answer: A: How should we merge the Chromosome and position columns of a vcf and or .map fil
4.9 years ago by WouterDeCoster 47k
0
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0
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774
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Answer: Answer: Problem to Read my file : infinite loop
updated 14 months ago by 43k • written 4.9 years ago by 47k
5
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2
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3.9k
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Answer: A: rename samples in a vcf or plink file
4.9 years ago by WouterDeCoster 47k
1
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0
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770
views
Answer: A: about GWAS studies and causal variants
4.9 years ago by WouterDeCoster 47k
3
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2
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1.1k
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Answer: A: Any help on how to detect viral transcripts in ONT RNAseq data
4.9 years ago by WouterDeCoster 47k
0
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1
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1.4k
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Answer: A: Validation of SNP and INDEL calling pipeline
5.0 years ago by WouterDeCoster 47k
0
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0
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733
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Answer: A: rna paired sequence sort is important
5.0 years ago by WouterDeCoster 47k
0
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0
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1.4k
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Answer: A: gatk HaplotypeCaller options
5.0 years ago by WouterDeCoster 47k
3
votes
3
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1.0k
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Answer: C: Split file not working
5.0 years ago by WouterDeCoster 47k
0
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1
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2.3k
views
Answer: A: Is it possible to merge/combine three genome into one?
5.0 years ago by WouterDeCoster 47k
4
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0
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12k
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Answer: A: QC of Oxford Nanopore fastq files with NanoPlot
5.0 years ago by WouterDeCoster 47k
1
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1
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1.0k
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Answer: A: separation of number of DE genes for one sample from output file obtain from ba
5.0 years ago by WouterDeCoster 47k
3
votes
1
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8.8k
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Answer: A: Oxford Nanopore error rate?
5.0 years ago by WouterDeCoster 47k
4
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0
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2.1k
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Answer: A: Benchmarking small variant calls: TP, FP, TN, FN
5.0 years ago by WouterDeCoster 47k
1
vote
0
replies
917
views
Answer: A: In which step should plink be used?
5.0 years ago by WouterDeCoster 47k
982 results • Page 3 of 20
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