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Answer: Answer: BBtools callvariants.sh
18 months ago by Brian Bushnell 20k
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0
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3.3k
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Answer: Answer: How to discard alignments from SAM/BAM file that have mismatches
18 months ago by Brian Bushnell 20k
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0
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1.5k
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Answer: Answer: Repeat detection/masking in bacteria
18 months ago by Brian Bushnell 20k
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1.2k
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Answer: Answer: Deduplication
18 months ago by Brian Bushnell 20k
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0
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3.4k
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Answer: Answer: Aligning very short sequences using bowtie2, I need fine control over how many m
18 months ago by Brian Bushnell 20k
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1.6k
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Answer: Answer: Mitochondrial contig identification in fungal genome assemblies
18 months ago by Brian Bushnell 20k
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652
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Answer: Answer: Partition reads in BAM file by MAG
18 months ago by Brian Bushnell 20k
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0
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2.7k
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Answer: Answer: Can BWA (mem) detect longer deletions?
18 months ago by Brian Bushnell 20k
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1.4k
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Answer: Answer: Average Coverage after Assembly (Spades)
18 months ago by Brian Bushnell 20k
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1
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1.1k
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Answer: Answer: Detect STRs in illumina library
18 months ago by Brian Bushnell 20k
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1
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3.5k
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Answer: Answer: What is the correct procedure to generate a consensus bacterial sequence?
18 months ago by Brian Bushnell 20k
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910
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Answer: Answer: Lower alignment rate when using collapsed reads
18 months ago by Brian Bushnell 20k
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1.4k
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Answer: Answer: Recommendations for extending contigs from denovo assembly to identify SV insert
18 months ago by Brian Bushnell 20k
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1
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6.9k
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Answer: Answer: Convert amino acid sequences into nucleotide sequences
18 months ago by Brian Bushnell 20k
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1
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1.2k
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Answer: Answer: Viral positive and negative strand with paired sequencing and bowtie
18 months ago by Brian Bushnell 20k
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0
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993
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Answer: Answer: How to choose the best tool for variant trio analysis
18 months ago by Brian Bushnell 20k
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2
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1.8k
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Answer: Answer: Aligner with statistics included?
updated 18 months ago by 45k • written 18 months ago by 20k
2
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1
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3.0k
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Answer: Answer: Building reference dbSNP file for citrus sinensis using 80 WGS samples
18 months ago by Brian Bushnell 20k
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0
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4.7k
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Answer: Answer: Which alignment for whole bacterial genomes for phylogenetic tree?
18 months ago by Brian Bushnell 20k
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0
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1.2k
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Answer: Answer: Estimating Index Hopping
18 months ago by Brian Bushnell 20k
1
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1
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1.5k
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Answer: Answer: checkstrand tool (from BBMap suite) question
updated 18 months ago by 151k • written 18 months ago by 20k
1
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3
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1.5k
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Answer: Answer: checkstrand tool (from BBMap suite) question
updated 18 months ago by 151k • written 18 months ago by 20k
3
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1
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2.1k
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Answer: Answer: Help with clumpify.sh
2.7 years ago by Brian Bushnell 20k
2
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1
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2.6k
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Answer: Answer: BBSplit index creation seems to use a subset of the references provided
2.9 years ago by Brian Bushnell 20k
3
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1
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3.1k
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Answer: C: BBMap tool error - randomreads.sh
4.4 years ago by Brian Bushnell 20k
4
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1
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2.7k
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Answer: A: Current challenges in SARS-CoV-2 analysis?
5.1 years ago by Brian Bushnell 20k
2
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2
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9.5k
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Answer: Answer: Calculate percentage of bases covered less than nX in targeted sequencing experi
updated 3.1 years ago by 45k • written 10.3 years ago by 20k
8
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0
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21k
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Answer: A: Extract sequence with header from a fasta file with specific ID given in another
updated 5.3 years ago by 45k • written 10.3 years ago by 20k
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0
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3.7k
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Answer: A: Extract only sequences that have N nucleotides
updated 5.3 years ago by 45k • written 9.3 years ago by 20k
1
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1
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5.5k
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Answer: A: samtools merge extremely slow
updated 5.4 years ago by 45k • written 9.3 years ago by 20k
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0
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1.7k
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Answer: A: Fast imputation of variants for 4x WGS?
updated 5.4 years ago by 45k • written 9.3 years ago by 20k
2
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0
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3.0k
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Answer: A: Extracting nucleotide immediately prior to mapped read
updated 5.4 years ago by 45k • written 9.3 years ago by 20k
4
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1
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13k
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Answer: A: How detrimental are duplicate reads in RNAseq experiments?
updated 5.4 years ago by 45k • written 9.3 years ago by 20k
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0
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1.6k
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Answer: A: Bowtie2 - Force alignment of terminal mismatches
updated 5.4 years ago by 45k • written 9.3 years ago by 20k
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0
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4.4k
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Answer: C: Does anyone know any specific 1000 genomes WGS data that is around 30x coverage?
updated 5.4 years ago by 45k • written 9.3 years ago by 20k
3
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0
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18k
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Answer: A: How to efficiently remove a list of reads from BAM file?
updated 5.4 years ago by 45k • written 9.3 years ago by 20k
1
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1
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4.7k
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Answer: A: Buying computational resources vs. renting allocation on cluster
updated 5.4 years ago by 45k • written 9.3 years ago by 20k
1
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1
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2.6k
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Answer: A: Assembly reads from only one file
updated 5.4 years ago by 45k • written 9.3 years ago by 20k
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1
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11k
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Answer: A: Looking for reputable tool to find low complexity regions in FASTQ or BAM files
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
1
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0
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3.7k
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Answer: A: get deletion coverage from .bam file
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
0
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1
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6.1k
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Answer: A: Plasmid Genome Assembly
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
3
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0
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3.7k
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Answer: A: Is it true that N50 is not an important parameter for quality in Transcriptome A
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
0
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0
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2.8k
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Answer: A: auto trimming of adapter and 8 base normalizing sequence from miRNA reads
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
2
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0
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2.1k
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Answer: A: Overlapping paired end read simulator
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
5
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2
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9.6k
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Answer: A: de novo sequence assembly with extremely high coverage
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
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0
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2.6k
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Answer: A: Viral Genome SNP and Indel Detection
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
1
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0
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6.2k
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Answer: A: Which aligner is best suited for circular human mitochondrial genome?
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
5
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1
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7.6k
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Answer: A: rRNA decontamination of RNA-Seq reads (tool choice, introns etc)
5.4 years ago by Brian Bushnell 20k
1
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3
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6.2k
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Answer: A: Lack of consensus between NGS & Sanger sequencing on indels/mutations
updated 5.4 years ago by 45k • written 9.4 years ago by 20k
2
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0
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3.7k
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Answer: A: Plotting Coverage - Strand specification
updated 5.4 years ago by 45k • written 9.5 years ago by 20k
632 results • Page 2 of 13
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