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Comment: C: Finding structural variants after Spades
5.1 years ago by WouterDeCoster 48k
0
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3.1k
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Comment: C: problem with trimmomatic
5.1 years ago by WouterDeCoster 48k
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Comment: C: Exome data processing and variant calling based on GRCH38
5.1 years ago by WouterDeCoster 48k
2
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1.4k
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Answer: A: Exome data processing and variant calling based on GRCH38
5.1 years ago by WouterDeCoster 48k
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879
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Comment: C: CRAM to amino acid based VCF
5.1 years ago by WouterDeCoster 48k
3
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2.3k
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Answer: A: Vcf normalization dificulties
5.1 years ago by WouterDeCoster 48k
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4.8k
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Comment: C: BWA mem and Samtools sort in Bash script
5.2 years ago by WouterDeCoster 48k
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1
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4.8k
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Comment: C: BWA mem and Samtools sort in Bash script
5.2 years ago by WouterDeCoster 48k
7
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1.2k
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Comment: C: How to make it significant
5.2 years ago by WouterDeCoster 48k
2
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1
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2.3k
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Comment: C: Place wordcount next to each word in a paragraph of text
5.2 years ago by WouterDeCoster 48k
0
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1
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2.3k
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Comment: C: Place wordcount next to each word in a paragraph of text
5.2 years ago by WouterDeCoster 48k
3
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2.3k
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Answer: A: Place wordcount next to each word in a paragraph of text
5.2 years ago by WouterDeCoster 48k
2
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1.1k
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Answer: A: how to choose some samples from a vcf files
5.2 years ago by WouterDeCoster 48k
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1.5k
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Comment: C: GENE BURDEN TEST
5.2 years ago by WouterDeCoster 48k
4
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1
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4.1k
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Answer: A: What is the best way to re-align a .bam file?
5.2 years ago by WouterDeCoster 48k
1
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1
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8.6k
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Answer: A: GATK Mutect2 Panel-Of-Normals generation
5.2 years ago by WouterDeCoster 48k
1
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1
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1.4k
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Comment: C: how can I find the download link for a famous dataset
5.2 years ago by WouterDeCoster 48k
1
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1
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1.7k
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Comment: C: Choice between Nanopore cDNA or direct RNA sequencing
5.2 years ago by WouterDeCoster 48k
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2
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2.2k
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Comment: C: minimap2: aligning ambigious sequence containing N to fastq reads.
5.2 years ago by WouterDeCoster 48k
1
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0
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2.8k
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Answer: A: How to calculate differential methylation from nanopore reads?
5.2 years ago by WouterDeCoster 48k
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1
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3.3k
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Comment: C: bcftools annotate from ID file in 1 VCF to an INFO field in another VCF
5.2 years ago by WouterDeCoster 48k
0
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1.1k
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Comment: C: Protein structural features and PSSM profile
5.3 years ago by WouterDeCoster 48k
0
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0
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977
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Comment: C: How to identify mRNAs, transcription start/stop sites and regulatory elements fr
5.3 years ago by WouterDeCoster 48k
1
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1
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1.2k
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Comment: C: MinION RNASeq data analysis
5.3 years ago by WouterDeCoster 48k
0
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0
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3.7k
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Comment: C: ONT fast5 basecalling
5.3 years ago by WouterDeCoster 48k
0
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1
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2.1k
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Comment: C: Problem to start Breakdancer
5.3 years ago by WouterDeCoster 48k
0
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0
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1.0k
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Comment: C: how to get fasta files for list of genes?
5.3 years ago by WouterDeCoster 48k
2
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7.4k
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Comment: C: how to run a tool (package) installed into anaconda environment ..using mac
5.3 years ago by WouterDeCoster 48k
0
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0
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1.5k
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Comment: C: Wild-Type and database SNPs effect
5.3 years ago by WouterDeCoster 48k
0
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0
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1.1k
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Comment: C: Finding enhancers of the whole human body
5.3 years ago by WouterDeCoster 48k
0
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1
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7.4k
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Comment: C: how to run a tool (package) installed into anaconda environment ..using mac
5.3 years ago by WouterDeCoster 48k
3
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1
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7.4k
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Comment: C: how to run a tool (package) installed into anaconda environment ..using mac
5.3 years ago by WouterDeCoster 48k
0
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0
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993
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Comment: C: What's the probability of genotype error at the end of 10 repeated A variants? G
5.3 years ago by WouterDeCoster 48k
1
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0
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7.4k
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Answer: A: how to run a tool (package) installed into anaconda environment ..using mac
5.3 years ago by WouterDeCoster 48k
0
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0
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978
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Answer: A: RNA-seq: indexing without sorting
5.3 years ago by WouterDeCoster 48k
0
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1
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1.0k
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Assemble and get consensus of inserted sequence
assembly structural variant nanopore
5.3 years ago by WouterDeCoster 48k
2
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0
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4.4k
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Answer: A: female with variant data in y chromosome
5.4 years ago by WouterDeCoster 48k
0
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1
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3.2k
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Comment: C: Workflow for structural variants from long read sequencing data
5.4 years ago by WouterDeCoster 48k
3
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1
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2.2k
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Answer: C: PCA plots and biological information taken from other principal components
5.4 years ago by WouterDeCoster 48k
0
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0
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2.3k
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Comment: C: mosdepth coverage so slow - fast way to get coverage of restricted regions WES
5.4 years ago by WouterDeCoster 48k
1
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1
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1.5k
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Answer: A: bcftools merge single-sample vcf files
5.4 years ago by WouterDeCoster 48k
1
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1
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9.2k
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Comment: C: NanoPack: Scripts for long read sequencing data processing and analysis: NanoPlo
5.4 years ago by WouterDeCoster 48k
2
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0
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894
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Answer: A: A few samples of read data
5.4 years ago by WouterDeCoster 48k
1
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2
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2.7k
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Comment: C: sethiyap/fastaR --> faSomeRecords was not found
5.4 years ago by WouterDeCoster 48k
1
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0
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1.7k
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Comment: C: Doubt regarding dna sequence length
5.4 years ago by WouterDeCoster 48k
4
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2
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1.7k
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Comment: C: Doubt regarding dna sequence length
5.4 years ago by WouterDeCoster 48k
0
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1
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2.2k
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Answer: A: WGCNA, analysis on two data sets
5.4 years ago by WouterDeCoster 48k
0
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0
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6.1k
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Comment: C: Minimap2 warning message
5.4 years ago by WouterDeCoster 48k
1
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0
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1.3k
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Comment: C: Counting speceficspecific lines that dosen't conaint speceficdon't contain speci
5.4 years ago by WouterDeCoster 48k
0
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1
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3.2k
views
Comment: C: Workflow for structural variants from long read sequencing data
5.4 years ago by WouterDeCoster 48k
7,263 results • Page 6 of 146
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