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Comment: Comment: Similar tools to visualize pileup of long-read alignments to a STR locus
8 weeks ago by WouterDeCoster 47k
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610
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Comment: Comment: validation approach for CNVs
5 months ago by WouterDeCoster 47k
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1
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785
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Comment: Comment: Identify and count gaps in sam/bam files
9 months ago by WouterDeCoster 47k
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2.0k
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Comment: Comment: pbmm2 alignment of long reads
9 months ago by WouterDeCoster 47k
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1
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788
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Comment: Comment: minimap2 U to T conversion
9 months ago by WouterDeCoster 47k
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1.5k
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Comment: Comment: Help aligning Nanopore Long Read RNA seqs
9 months ago by WouterDeCoster 47k
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1
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1.5k
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Comment: Comment: Help aligning Nanopore Long Read RNA seqs
9 months ago by WouterDeCoster 47k
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1
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603
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Comment: Comment: vcf phasing
10 months ago by WouterDeCoster 47k
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662
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Comment: Comment: Filter BAM to keep only alignments at an interval, ignoring reads spliced over
11 months ago by WouterDeCoster 47k
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3
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662
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Filter BAM to keep only alignments at an interval, ignoring reads spliced over
samtools bam splicing
11 months ago by WouterDeCoster 47k
2
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1
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2.0k
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Answer: Answer: Is it possible to access the code of a bioinformatics article?
14 months ago by WouterDeCoster 47k
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1.1k
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Comment: Comment: Find reference fasta based on M5/MD5 string
14 months ago by WouterDeCoster 47k
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1.1k
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Comment: Comment: Find reference fasta based on M5/MD5 string
14 months ago by WouterDeCoster 47k
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1.5k
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Comment: Comment: Isolating and extracting regions in VCF file
14 months ago by WouterDeCoster 47k
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4
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1.1k
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Find reference fasta based on M5/MD5 string
reference fasta
14 months ago by WouterDeCoster 47k
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0
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887
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Comment: Comment: Re-format sample columns in VCF file
14 months ago by WouterDeCoster 47k
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1
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2.5k
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Comment: Comment: ONT Raw Read Sequencing Pipeline
14 months ago by WouterDeCoster 47k
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1
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1.4k
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Comment: Comment: somatic variant calling without matched normal in long-reads
14 months ago by WouterDeCoster 47k
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1
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2.5k
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Comment: Comment: ONT Raw Read Sequencing Pipeline
14 months ago by WouterDeCoster 47k
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1
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2.5k
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Comment: Comment: ONT Raw Read Sequencing Pipeline
14 months ago by WouterDeCoster 47k
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1
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3.3k
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Comment: Comment: How to speed Salmon index up
14 months ago by WouterDeCoster 47k
2
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1
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1.9k
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Comment: Comment: Snakemake rule error
15 months ago by WouterDeCoster 47k
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0
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714
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Comment: Comment: how do I assemble centromere regions in a plant genome?
16 months ago by WouterDeCoster 47k
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637
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Comment: Comment: DOES MGI SEQUENCING RESULT CONTAINS MULTIPLE FILES FOR SINGLE SAMPLE
16 months ago by WouterDeCoster 47k
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0
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3.4k
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Comment: Comment: How to remove fasta headers in a multifasta file and write file name as a fasta
19 months ago by WouterDeCoster 47k
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0
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1.4k
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Comment: Comment: Expected number of raw reads in fq.gz files in PE sequencing
19 months ago by WouterDeCoster 47k
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0
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433
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Number of reads per gene in pseudobulk with more or fewer nuclei
nuclei 10x sequencing
19 months ago by WouterDeCoster 47k
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1
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3.4k
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Comment: Comment: Create a reference genome from aligned bam file
19 months ago by WouterDeCoster 47k
2
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1
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2.0k
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Comment: Comment: Batch correction for Nanopore RNAseq
21 months ago by WouterDeCoster 47k
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0
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1.1k
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Comment: Comment: Extract samples from a VCF file that contain marker
21 months ago by WouterDeCoster 47k
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1
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940
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Answer: Answer: rust_htslib unrecognized filter ID
21 months ago by WouterDeCoster 47k
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0
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889
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Answer: Answer: Truvari error: Failed to parse TBX_VCF - "ead mapping qualities">"
21 months ago by WouterDeCoster 47k
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0
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715
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Comment: Comment: Pairwise Alignment
22 months ago by WouterDeCoster 47k
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1
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4.3k
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Comment: Comment: minimap's SAM file MAPQ value for the unique alignments
22 months ago by WouterDeCoster 47k
1
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0
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835
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Comment: Comment: Colleges
22 months ago by WouterDeCoster 47k
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1
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1.4k
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Answer: Answer: SyntaxError (Perhaps you forgot a comma?) in snakefile when running FastQC.
22 months ago by WouterDeCoster 47k
1
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0
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1.1k
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Comment: Comment: rna long read length distibution
22 months ago by WouterDeCoster 47k
0
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0
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799
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Comment: Comment: Mapping reads to a multifasta reference
22 months ago by WouterDeCoster 47k
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1
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1.5k
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Comment: Comment: Estimate sizes of repeats in a especific Gene
22 months ago by WouterDeCoster 47k
1
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0
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2.9k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
22 months ago by WouterDeCoster 47k
1
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1
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2.9k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
22 months ago by WouterDeCoster 47k
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0
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2.7k
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Comment: Comment: Nanopore config files
22 months ago by WouterDeCoster 47k
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1
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2.7k
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Answer: Answer: Nanopore config files
22 months ago by WouterDeCoster 47k
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0
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808
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Comment: Comment: Change VCF File Reference Genome to a Local .FA File
23 months ago by WouterDeCoster 47k
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1
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1.4k
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Comment: Comment: problem with bedtools getfasta
23 months ago by WouterDeCoster 47k
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0
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1.2k
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Answer: Answer: htseq-count : dosen't show options in bash ln ubuntu
23 months ago by WouterDeCoster 47k
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0
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1.6k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
24 months ago by WouterDeCoster 47k
3
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0
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1.6k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
24 months ago by WouterDeCoster 47k
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1
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1.6k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
24 months ago by WouterDeCoster 47k
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1
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1.7k
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Comment: Comment: How can I generate VCF file with two different assembled genome fasta?
24 months ago by WouterDeCoster 47k
7,262 results • Page 1 of 146
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