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Comment: Comment: Similar tools to visualize pileup of long-read alignments to a STR locus
4 months ago by WouterDeCoster 48k
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792
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Comment: Comment: validation approach for CNVs
8 months ago by WouterDeCoster 48k
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1
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952
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Comment: Comment: Identify and count gaps in sam/bam files
11 months ago by WouterDeCoster 48k
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1
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2.5k
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Comment: Comment: pbmm2 alignment of long reads
11 months ago by WouterDeCoster 48k
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1
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976
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Comment: Comment: minimap2 U to T conversion
12 months ago by WouterDeCoster 48k
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1.8k
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Comment: Comment: Help aligning Nanopore Long Read RNA seqs
12 months ago by WouterDeCoster 48k
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1
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1.8k
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Comment: Comment: Help aligning Nanopore Long Read RNA seqs
12 months ago by WouterDeCoster 48k
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1
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792
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Comment: Comment: vcf phasing
13 months ago by WouterDeCoster 48k
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797
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Comment: Comment: Filter BAM to keep only alignments at an interval, ignoring reads spliced over
13 months ago by WouterDeCoster 48k
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3
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797
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Filter BAM to keep only alignments at an interval, ignoring reads spliced over
samtools bam splicing
13 months ago by WouterDeCoster 48k
2
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1
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2.4k
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Answer: Answer: Is it possible to access the code of a bioinformatics article?
16 months ago by WouterDeCoster 48k
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1.3k
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Comment: Comment: Find reference fasta based on M5/MD5 string
17 months ago by WouterDeCoster 48k
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1.3k
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Comment: Comment: Find reference fasta based on M5/MD5 string
17 months ago by WouterDeCoster 48k
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1.8k
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Comment: Comment: Isolating and extracting regions in VCF file
17 months ago by WouterDeCoster 48k
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4
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1.3k
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Find reference fasta based on M5/MD5 string
reference fasta
17 months ago by WouterDeCoster 48k
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0
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1.1k
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Comment: Comment: Re-format sample columns in VCF file
17 months ago by WouterDeCoster 48k
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1
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2.8k
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Comment: Comment: ONT Raw Read Sequencing Pipeline
17 months ago by WouterDeCoster 48k
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1
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1.6k
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Comment: Comment: somatic variant calling without matched normal in long-reads
17 months ago by WouterDeCoster 48k
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1
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2.8k
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Comment: Comment: ONT Raw Read Sequencing Pipeline
17 months ago by WouterDeCoster 48k
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1
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2.8k
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Comment: Comment: ONT Raw Read Sequencing Pipeline
17 months ago by WouterDeCoster 48k
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1
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4.0k
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Comment: Comment: How to speed Salmon index up
17 months ago by WouterDeCoster 48k
2
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1
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2.2k
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Comment: Comment: Snakemake rule error
18 months ago by WouterDeCoster 48k
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0
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904
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Comment: Comment: how do I assemble centromere regions in a plant genome?
19 months ago by WouterDeCoster 48k
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790
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Comment: Comment: DOES MGI SEQUENCING RESULT CONTAINS MULTIPLE FILES FOR SINGLE SAMPLE
19 months ago by WouterDeCoster 48k
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0
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3.7k
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Comment: Comment: How to remove fasta headers in a multifasta file and write file name as a fasta
21 months ago by WouterDeCoster 48k
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0
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1.7k
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Comment: Comment: Expected number of raw reads in fq.gz files in PE sequencing
22 months ago by WouterDeCoster 48k
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0
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555
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Number of reads per gene in pseudobulk with more or fewer nuclei
nuclei 10x sequencing
22 months ago by WouterDeCoster 48k
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1
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3.9k
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Comment: Comment: Create a reference genome from aligned bam file
22 months ago by WouterDeCoster 48k
2
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1
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2.2k
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Comment: Comment: Batch correction for Nanopore RNAseq
24 months ago by WouterDeCoster 48k
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0
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1.2k
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Comment: Comment: Extract samples from a VCF file that contain marker
24 months ago by WouterDeCoster 48k
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1
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1.1k
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Answer: Answer: rust_htslib unrecognized filter ID
24 months ago by WouterDeCoster 48k
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0
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1.0k
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Answer: Answer: Truvari error: Failed to parse TBX_VCF - "ead mapping qualities">"
2.0 years ago by WouterDeCoster 48k
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0
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827
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Comment: Comment: Pairwise Alignment
2.0 years ago by WouterDeCoster 48k
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1
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4.7k
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Comment: Comment: minimap's SAM file MAPQ value for the unique alignments
2.0 years ago by WouterDeCoster 48k
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0
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1.0k
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Comment: Comment: Colleges
2.0 years ago by WouterDeCoster 48k
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1
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1.5k
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Answer: Answer: SyntaxError (Perhaps you forgot a comma?) in snakefile when running FastQC.
2.1 years ago by WouterDeCoster 48k
1
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0
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1.4k
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Comment: Comment: rna long read length distibution
2.1 years ago by WouterDeCoster 48k
0
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0
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942
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Comment: Comment: Mapping reads to a multifasta reference
2.1 years ago by WouterDeCoster 48k
0
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1
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1.7k
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Comment: Comment: Estimate sizes of repeats in a especific Gene
2.1 years ago by WouterDeCoster 48k
1
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0
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3.3k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
2.1 years ago by WouterDeCoster 48k
1
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1
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3.3k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
2.1 years ago by WouterDeCoster 48k
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0
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3.2k
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Comment: Comment: Nanopore config files
2.1 years ago by WouterDeCoster 48k
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1
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3.2k
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Answer: Answer: Nanopore config files
2.1 years ago by WouterDeCoster 48k
0
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0
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948
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Comment: Comment: Change VCF File Reference Genome to a Local .FA File
2.1 years ago by WouterDeCoster 48k
0
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1
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1.5k
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Comment: Comment: problem with bedtools getfasta
2.2 years ago by WouterDeCoster 48k
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0
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1.4k
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Answer: Answer: htseq-count : dosen't show options in bash ln ubuntu
2.2 years ago by WouterDeCoster 48k
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0
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1.9k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
2.2 years ago by WouterDeCoster 48k
3
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0
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1.9k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
2.2 years ago by WouterDeCoster 48k
0
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1
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1.9k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
2.2 years ago by WouterDeCoster 48k
0
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1
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1.9k
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Comment: Comment: How can I generate VCF file with two different assembled genome fasta?
2.2 years ago by WouterDeCoster 48k
7,262 results • Page 1 of 146
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