Genome indexing
What are the different tools we can use for genome indexing?
Thanks
genomeindexing
indexing
• 1,319 views
•
link
updated
by
Marco Pannone •
•
written
by
Roy.anupama11 •
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
align_and_estimate_abundance.pl
written by Roy.anupama11 •In `align_and_estimate_abundance.pl` script can we use both paired end and single end data at the same run? Or we need to execute them separately?
-
How does Indexing and de-novo identification and masking of repetitive elements occurs?
written by Roy.anupama11 •In order to identify and masks the repetitive elements from my reference genome. What and how I should proceed with the tools RepeatModeler and RepeatMasker? …
-
Best Pipeline for De novo transcriptome SC-RNAseq
written by Chris •Hi everyone, I'm curious what the best pipeline for single cell RNA seq is if your organism of interest doesn't have a genome. Tools such …
-
How to search and identify the function of DEGs
written by Roy.anupama11 •How to retrieve and identify the function of DEGs? What are the different types of tools available?
-
tools for alignment and methylation extraction for MeDIP sequencing
written by ruchi19sinha •For methylation study in cancer, we have MeDIP-seq data. What are all tools that we can use for alignment and calling methylation. Can Bismark be …
-
Causation between two genome annotations
written by Eamag •I have one-dimentional array (human genome). Also I have two annotations for it, we can think about them as different peaks (it's nucleosome and secondary …
-
Issues with building an index in salmon
written by oma219 •Hello, I was building an index with Salmon and had some of these warnings come up with the index was being built. Are these warnings …
-
Multiple genome alignment
written by gladyHello friends, can anyone tell me what is the purpose of doing multiple genome alignment ? Which are the different tools we can use for …
-
bowtie, tophat vs BLAST
written by niu2rseqHi, I have a very basic question but it confused me a little bit. For a metatranscriptome data, we can compare it with the NCBI …
-
Snp Calling Tools And Costs
written by Andrea_Bio •<p>Hello</p> <p>Please can you tell me what are the main software tools people in the industry use for snp calling and to obtain whole genome …
Very vague question, it depends on what you are going to do afterward.
Supposing you have a genome in .fasta format and you are going to align some sequencing data, you need to index it with the specific tool you are using for alignment.
Examples: Bowtie2; HISAT2.
Actually I came across Picard (https://github.com/broadinstitute/picard) and BWA. I wanted to re-confirm. Since I never used both. I have used HISAT2. Instead of BWA, can I use HISAT2?
What type of data do you have? RNA-seq?