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Comment: Comment: How can I generate VCF file with two different assembled genome fasta?
2.6 years ago by WouterDeCoster 48k
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1
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2.2k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
2.6 years ago by WouterDeCoster 48k
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2.2k
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Comment: Comment: featureCounts problem in reading Gff
2.7 years ago by WouterDeCoster 48k
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1
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2.2k
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Comment: Comment: featureCounts problem in reading Gff
2.7 years ago by WouterDeCoster 48k
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1.5k
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Comment: Comment: Bioinformatics package
2.7 years ago by WouterDeCoster 48k
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2.0k
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Comment: Comment: Trying to make a Mauve alignment with 2 sequences and keep getting error code 3
2.7 years ago by WouterDeCoster 48k
2
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1.1k
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Answer: Answer: N50 value is equal to the single contig?
2.7 years ago by WouterDeCoster 48k
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5.6k
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Answer: Answer: long read + salmon? (transcript abundance)
2.7 years ago by WouterDeCoster 48k
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8.2k
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Answer: Answer: Filtering out the spliced reads from bam file.
2.9 years ago by WouterDeCoster 48k
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5.0k
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Comment: Comment: Transform Data into DNA picture
3.0 years ago by WouterDeCoster 48k
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1.2k
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Comment: Comment: Looking for incompatible packages
3.0 years ago by WouterDeCoster 48k
4
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1
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5.0k
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Comment: Comment: Transform Data into DNA picture
3.0 years ago by WouterDeCoster 48k
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2.5k
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Comment: Comment: Introducing Cramino: a *fast* QC tool for long reads
3.0 years ago by WouterDeCoster 48k
4
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2
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2.5k
views
Tool: Introducing Cramino: a *fast* QC tool for long reads
long-read nanopore pacbio
updated 19 months ago by 45k • written 3.1 years ago by 48k
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1
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1.9k
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Comment: Comment: How to calculate the depth of nanopore reads in IGV
3.1 years ago by WouterDeCoster 48k
0
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1
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1.5k
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Comment: Comment: how to get a sequence from read fragments with ref sequence?
3.4 years ago by WouterDeCoster 48k
0
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1
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1.5k
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Comment: Comment: Subsetting VCF file - error in script?
3.4 years ago by WouterDeCoster 48k
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0
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2.1k
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Comment: Comment: how to align an intron from a complex
3.4 years ago by WouterDeCoster 48k
0
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1
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1.5k
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Answer: Answer: Subsetting VCF file - error in script?
3.4 years ago by WouterDeCoster 48k
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0
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2.1k
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Comment: Comment: bcftools stats: definition of indel type
3.5 years ago by WouterDeCoster 48k
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0
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2.1k
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Comment: Comment: bcftools stats: definition of indel type
3.5 years ago by WouterDeCoster 48k
1
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5
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2.1k
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bcftools stats: definition of indel type
vcf bcftools
3.5 years ago by WouterDeCoster 48k
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1
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1.0k
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Answer: Answer: IGV base counts do not add up to total count
3.6 years ago by WouterDeCoster 48k
2
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1
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2.0k
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Comment: Comment: CNV - Copy number variations. Which tool is most used for?
3.6 years ago by WouterDeCoster 48k
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1
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1.5k
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Comment: Comment: Bash loop one liner
3.7 years ago by WouterDeCoster 48k
0
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1
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1.0k
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Comment: Comment: Brain code
3.7 years ago by WouterDeCoster 48k
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2
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1.8k
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Comment: Comment: 1000 genomes data?
3.7 years ago by WouterDeCoster 48k
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0
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1.4k
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Answer: Answer: New graduate student in Computational Biology, confused by reads versus copy num
3.7 years ago by WouterDeCoster 48k
4
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2
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2.1k
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Use bcftools to find carriers of variants
vcf bcftools
updated 3.7 years ago by 166k • written 3.7 years ago by 48k
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973
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Comment: Comment: Error when I tried to: Add Read group information and align PE reads to the wh
3.8 years ago by WouterDeCoster 48k
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1
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4.4k
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Answer: Answer: What does an amino acid sequence that does not start with methionine mean?
3.8 years ago by WouterDeCoster 48k
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0
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2.3k
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Comment: Comment: Guppy Aligner/Samtools -- Parse error in SAM file
3.8 years ago by WouterDeCoster 48k
0
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0
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2.3k
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Comment: Comment: Strange error when using gzip.open with a VCF file
3.8 years ago by WouterDeCoster 48k
1
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1
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19k
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Comment: Comment: QC of Oxford Nanopore fastq files with NanoPlot
3.8 years ago by WouterDeCoster 48k
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1
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1.7k
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Comment: Comment: number of exons
3.8 years ago by WouterDeCoster 48k
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0
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2.9k
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Comment: Comment: Using Nanoplot to asses quality of ONT data
3.8 years ago by WouterDeCoster 48k
0
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1
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2.9k
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Comment: Comment: Using Nanoplot to asses quality of ONT data
3.8 years ago by WouterDeCoster 48k
0
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1
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1.3k
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Comment: Comment: SNP associated contigs
3.9 years ago by WouterDeCoster 48k
0
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1
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1.7k
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Comment: Comment: Software for multiple sequence alignment?
3.9 years ago by WouterDeCoster 48k
1
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1
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1.7k
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Comment: Comment: Software for multiple sequence alignment?
3.9 years ago by WouterDeCoster 48k
2
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1
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6.1k
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Comment: Comment: In 2022 is Perl and Ruby programming languages still useful for bioinformatics?
3.9 years ago by WouterDeCoster 48k
2
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2
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2.9k
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Comment: Comment: Snakemake: MissingInputException
4.0 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Comment: Comment: Most useful public genomic/genetic databases/tools/applications
4.0 years ago by WouterDeCoster 48k
0
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1
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3.2k
views
Comment: Comment: Most useful public genomic/genetic databases/tools/applications
4.0 years ago by WouterDeCoster 48k
1
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1
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3.2k
views
Comment: Comment: Most useful public genomic/genetic databases/tools/applications
4.0 years ago by WouterDeCoster 48k
0
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0
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1.8k
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Comment: Comment: Computational Biology Conference
4.0 years ago by WouterDeCoster 48k
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0
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12k
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Comment: Comment: How filter genes to construct co-expression network?
4.0 years ago by WouterDeCoster 48k
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0
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2.2k
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Comment: Comment: Having trouble converting gene names to Ensemble ID using biomaRt
4.0 years ago by WouterDeCoster 48k
0
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0
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4.6k
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Comment: Comment: Pysam & VCF: How to add sample information to a new record?
4.0 years ago by WouterDeCoster 48k
3
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1
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2.2k
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Answer: Answer: Having trouble converting gene names to Ensemble ID using biomaRt
4.0 years ago by WouterDeCoster 48k
7,263 results • Page 2 of 146
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