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Comment: C: What tool should I use for the identification of DNA transposons?
4.7 years ago by lakhujanivijay 5.9k
0
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1
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1.3k
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Answer: A: What tool should I use for the identification of DNA transposons?
4.7 years ago by lakhujanivijay 5.9k
2
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1
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2.8k
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Answer: A: volcano plot in R
4.7 years ago by lakhujanivijay 5.9k
1
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0
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1.1k
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Answer: A: Reference of Whole exome sequecing analysis
4.7 years ago by lakhujanivijay 5.9k
2
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0
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3.6k
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Answer: A: FASTA file split
4.7 years ago by lakhujanivijay 5.9k
0
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0
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2.3k
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Answer: A: Batch rename protein fasta headers
4.7 years ago by lakhujanivijay 5.9k
0
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0
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880
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Answer: A: Plot per base coverage from regions coverage with R
4.7 years ago by lakhujanivijay 5.9k
0
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1
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1.4k
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Comment: C: Same fastqs and pipeline get different variant results
4.7 years ago by lakhujanivijay 5.9k
0
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1
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1.0k
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Comment: C: script to print fasta file
4.8 years ago by lakhujanivijay 5.9k
0
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1
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3.3k
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Comment: C: Quick way to annotate a target exome BED file with gene name information
4.8 years ago by lakhujanivijay 5.9k
0
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1
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3.3k
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Comment: C: Quick way to annotate a target exome BED file with gene name information
4.8 years ago by lakhujanivijay 5.9k
1
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0
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883
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Answer: C: creating chromosome plot
4.8 years ago by lakhujanivijay 5.9k
0
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8
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3.3k
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Quick way to annotate a target exome BED file with gene name information
exon bed annotate gene
4.8 years ago by lakhujanivijay 5.9k
0
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0
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14k
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Comment: C: How to create a Fasta file using info from a Excel file
4.8 years ago by lakhujanivijay 5.9k
3
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0
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5.2k
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Comment: C: converting taxID to taxonomy
4.8 years ago by lakhujanivijay 5.9k
0
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0
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1.2k
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Comment: C: How to integrate custom variant callers for consensus genotyping using CGES?
4.9 years ago by lakhujanivijay 5.9k
0
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2
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1.2k
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How to integrate custom variant callers for consensus genotyping using CGES?
cges consens genotyping germline variant
4.9 years ago by lakhujanivijay 5.9k
0
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0
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14k
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Comment: C: How to assemble contigs?
4.9 years ago by lakhujanivijay 5.9k
1
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6
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3.2k
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Is there any way to download knownCanonical set from the NCBI Refseq track as it is possible for the UCSC track ?
ucsc canonical refseq table browser hg19
updated 4.9 years ago by ▴ 10 • written 4.9 years ago by 5.9k
0
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0
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13k
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Comment: C: How to install samtools v.1.2 on Ubuntu 14.0 32 bit?
updated 4.9 years ago by 44k • written 5.7 years ago by 5.9k
0
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1
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3.2k
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Comment: C: Is there any way to download knownCanonical set from the NCBI Refseq track as it
4.9 years ago by lakhujanivijay 5.9k
1
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0
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1.6k
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Answer: A: What do you think of sci-hub?
4.9 years ago by lakhujanivijay 5.9k
1
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0
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1.9k
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Comment: C: how to use output of cnvkit to plot
5.0 years ago by lakhujanivijay 5.9k
0
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0
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3.6k
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Comment: C: to calculate coverage of each contig after assembly
5.0 years ago by lakhujanivijay 5.9k
0
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1
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160k
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Comment: C: The Biostar Handbook. A bioinformatics e-book for beginners.
5.0 years ago by lakhujanivijay 5.9k
1
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1
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1.5k
views
How to adjust/add cytoband information in specific regions of karyoplot?
karyoploter cnv bioconductor R
updated 5.0 years ago by 12k • written 5.0 years ago by 5.9k
1
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2
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947
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Is there any way to avoid adding the PG tag while creating a SAM output from BWA ?
bwa sam pg
updated 5.0 years ago by 104k • written 5.0 years ago by 5.9k
0
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1
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9.6k
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Comment: C: bcftools variant filteration
5.0 years ago by lakhujanivijay 5.9k
1
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0
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2.5k
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Comment: C: Hadoop BAM - how to use?
updated 5.0 years ago by 86k • written 5.0 years ago by 5.9k
6
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3
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4.2k
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How to create Illumina sample sheet file for single index data?
illumina novaseq single index bcl2fastq
updated 5.1 years ago by 148k • written 5.1 years ago by 5.9k
0
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0
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4.2k
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Comment: C: How to create Illumina sample sheet file for single index data?
5.1 years ago by lakhujanivijay 5.9k
1
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1
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821
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Answer: A: Discrepancy in number of BLAST hits
5.1 years ago by lakhujanivijay 5.9k
1
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1
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3.3k
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Comment: C: Delta CT in R
5.1 years ago by lakhujanivijay 5.9k
0
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1
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2.2k
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Comment: C: Whole genome sequencing or whole exome sequencing- which is better and why?
5.1 years ago by lakhujanivijay 5.9k
1
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0
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6.5k
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Comment: C: sra-toolkit and fastq-dump error
5.1 years ago by lakhujanivijay 5.9k
0
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1
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1.2k
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Comment: C: SnpEff question for Variant annotation
5.1 years ago by lakhujanivijay 5.9k
3
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0
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5.1k
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Answer: A: How to automate bcl2fastq such that it is launched every time the run finishes o
5.1 years ago by lakhujanivijay 5.9k
0
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2
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1.3k
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Comment: C: error in trinty
5.1 years ago by lakhujanivijay 5.9k
0
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0
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1.8k
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Comment: C: WGCNA for RNA-SEQ DATA
5.1 years ago by lakhujanivijay 5.9k
0
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1
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3.9k
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Comment: C: Bioinformatics tutor good in Python
5.1 years ago by lakhujanivijay 5.9k
20
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11
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5.1k
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How to automate bcl2fastq such that it is launched every time the run finishes off on Illumina sequencer?
illumina bcl2fastq automation
updated 5.1 years ago by 8.3k • written 5.2 years ago by 5.9k
0
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1
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3.0k
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Comment: C: Tassel5v2 vcf file with 'N' in reference and alternate allele
5.1 years ago by lakhujanivijay 5.9k
4
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1
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3.5k
views
Answer: A: Which aligners are commonly used for DNA-seq data alignment?
5.1 years ago by lakhujanivijay 5.9k
1
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1
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2.3k
views
Comment: C: Confusing RNA-seq Alignment Stats (HISAT2 & Qualimap)
5.1 years ago by lakhujanivijay 5.9k
1
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0
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8.2k
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Comment: C: Samtools flagstat number of reads do not match actual total number of reads.
5.2 years ago by lakhujanivijay 5.9k
0
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0
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965
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Comment: C: tools for alignment and methylation extraction for MeDIP sequencing
5.2 years ago by lakhujanivijay 5.9k
0
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1
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9.5k
views
Comment: A: Ion Torrent Fastq Format Type?
5.2 years ago by lakhujanivijay 5.9k
3
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1
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1.5k
views
Answer: A: Use of export command
5.2 years ago by lakhujanivijay 5.9k
1
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0
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3.3k
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Comment: C: Genome size estimation using Kmergenie
5.2 years ago by lakhujanivijay 5.9k
0
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2
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2.5k
views
How to check for contamination and separate the data?
WGS bacteriophage
updated 5.2 years ago by ▴ 280 • written 8.4 years ago by 5.9k
895 results • Page 2 of 18
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