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1
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Answer: A: Correlation between coverage and variant calling
4.8 years ago by harish ▴ 470
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1.3k
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Answer: A: found non conserved regions between 2 genomes
4.9 years ago by harish ▴ 470
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6.3k
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Answer: A: best kmer for genome size estimation
5.0 years ago by harish ▴ 470
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3
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22k
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Answer: A: Polish PacBio assembly with latest PacBio tools : an affordable solution for eve
5.1 years ago by harish ▴ 470
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1.2k
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Answer: A: Best tool for variant calling in polyploids
5.1 years ago by harish ▴ 470
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1.6k
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Comment: C: How to subset bamfile based on chromosome IDs
5.1 years ago by harish ▴ 470
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1
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6.9k
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Answer: A: Alternative to BLASR ?
5.2 years ago by harish ▴ 470
4
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23k
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Answer: A: VCF merge or concatenate?
5.4 years ago by harish ▴ 470
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3.1k
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Comment: A: Is it possible to use genomic reads from PacBio and Nanopore with Illumina RNA-s
5.5 years ago by harish ▴ 470
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1.7k
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Comment: C: Using 10X Chromium linked reads for genome gap-filling
5.5 years ago by harish ▴ 470
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2.6k
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Comment: C: Kronagram from Kraken2 output?
5.5 years ago by harish ▴ 470
1
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1.7k
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Answer: A: Using 10X Chromium linked reads for genome gap-filling
5.5 years ago by harish ▴ 470
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2.6k
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Comment: A: Kronagram from Kraken2 output?
5.5 years ago by harish ▴ 470
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3.3k
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Comment: C: Genome assembly contig ordering
5.5 years ago by harish ▴ 470
2
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4.4k
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Answer: A: Assembler for only nanopore data
5.6 years ago by harish ▴ 470
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1
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3.4k
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Comment: C: Enhancing draft genome using 10X data
5.6 years ago by harish ▴ 470
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1.9k
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Answer: A: inputs to genomicconsensus arrow algorithm
5.7 years ago by harish ▴ 470
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4.1k
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Comment: C: Can I use two restriction enzymes to analyze HiC data using HiCExplorer
5.7 years ago by harish ▴ 470
2
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1
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4.1k
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Answer: A: Can I use two restriction enzymes to analyze HiC data using HiCExplorer
5.7 years ago by harish ▴ 470
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1
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3.4k
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Comment: C: Enhancing draft genome using 10X data
5.7 years ago by harish ▴ 470
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3.4k
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Comment: C: Enhancing draft genome using 10X data
5.7 years ago by harish ▴ 470
0
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2.3k
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Answer: A: merging 10X genomics assemblies
5.7 years ago by harish ▴ 470
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1
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3.4k
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Comment: C: Enhancing draft genome using 10X data
5.7 years ago by harish ▴ 470
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1.3k
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Comment: C: Extract fasta-headers that have the same word
5.7 years ago by harish ▴ 470
1
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34k
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Comment: A: How to systematically check if a bam file is truncated
5.8 years ago by harish ▴ 470
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6.9k
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Comment: C: Alternative to BLASR ?
5.9 years ago by harish ▴ 470
1
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1
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3.4k
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Comment: C: Enhancing draft genome using 10X data
5.9 years ago by harish ▴ 470
1
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1
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6.9k
views
Comment: C: Alternative to BLASR ?
5.9 years ago by harish ▴ 470
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0
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1.8k
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Answer: A: Protein categorization using COG
6.1 years ago by harish ▴ 470
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0
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4.1k
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Answer: A: Is there no way to bypass the Windows requirement for working with Thermo RAW fi
6.1 years ago by harish ▴ 470
0
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1
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3.8k
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Comment: C: Issues with mapping reads onto Reference genome using bwa mem
6.2 years ago by harish ▴ 470
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3.4k
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Comment: C: Using RNA-seq reads from closely related species in BRAKER2 genome annotation pi
6.2 years ago by harish ▴ 470
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1
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3.4k
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Comment: C: Using RNA-seq reads from closely related species in BRAKER2 genome annotation pi
6.2 years ago by harish ▴ 470
3
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1
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4.3k
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Answer: A: What is the next step after download the ncbi sra data of pacbio RSII sequencing
6.2 years ago by harish ▴ 470
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0
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2.1k
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Answer: A: Options for long-read diploid assembly
6.2 years ago by harish ▴ 470
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0
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4.6k
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Comment: C: Why learn programming in bioinformatics?
6.2 years ago by harish ▴ 470
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2
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4.0k
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Answer: A: Visualizing contig alignment
6.2 years ago by harish ▴ 470
1
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1
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2.0k
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Comment: C: How can I get only the rows when for the converge points : - +
6.2 years ago by harish ▴ 470
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1.9k
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Answer: A: Gene ontology analysis
6.2 years ago by harish ▴ 470
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0
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24k
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Answer: A: Assessing The Quality Of De Novo Assembled Data
6.3 years ago by harish ▴ 470
2
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2
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3.4k
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Answer: A: Using RNA-seq reads from closely related species in BRAKER2 genome annotation pi
6.3 years ago by harish ▴ 470
0
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1
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2.7k
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Comment: C: Metagenomic classification by custom database
6.3 years ago by harish ▴ 470
1
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1
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1.1k
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Answer: A: Are scaffolds in published draft genomes always ordered?
6.3 years ago by harish ▴ 470
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1
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1.8k
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Answer: A: obtaining a concatenamer of sequences
6.3 years ago by harish ▴ 470
1
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1
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5.0k
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Comment: C: To reassemble Illumina and PacBio, or just upgrade previous assembly with PacBio
6.3 years ago by harish ▴ 470
1
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0
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7.6k
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Answer: A: What does interproscan add to gene annotation?
6.3 years ago by harish ▴ 470
6
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1
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19k
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Answer: A: Remove sequences <300 bases from FASTA file
updated 6.3 years ago by 44k • written 6.3 years ago by ▴ 470
0
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0
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1.9k
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Comment: C: puzzled about "-kmer" options during de novo assembly
6.3 years ago by harish ▴ 470
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1
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19k
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Comment: C: Remove sequences <300 bases from FASTA file
6.3 years ago by harish ▴ 470
0
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4.4k
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Comment: C: Merging multiple sets of transcripts (generated by Trinity)
6.3 years ago by harish ▴ 470
56 results • Page 1 of 2
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