Is It Necessary To Remove Duplications After Bwa Alignment?
HI, I got another question here, is it always necessary to find duplicates and remove them after bWA alignment whatever alignment is good or not?
bwa
• 5,108 views
•
link
written
by
Tonyzeng •
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
A Quick Way To View Or Check The Order Of Chromosome In Bam File
written by Tonyzeng •<p>HI I have question here, if I just need to check or view the order of chromosome in <a href='http://samtools.sourceforge.net/SAM1.pdf'>BAM</a> file after aligment with <a …
-
Need Suggestions For The Sequencing Data Analysis From Mouse Community
written by Tonyzeng •<p>HI, I am new in next generation sequencing data analysis (exome sequencing) in mouse community, Very appreciated for giving me any suggestions if you have …
-
Bwa Alignment And Input Pair-End Format, Does Fastq Encoding Of The Input Matter?
written by Tonyzeng •<p>Hi, I am curious about a question. I have pair-end reads here as T1.fq and T2.fq (fastq format) that are produced by illumina 1.8. When …
-
Bwa Index Output And Bwa Aln Problem
written by Tonyzeng •<p>My output of <a href='http://bio-bwa.sourceforge.net/'>BWA</a> index has only 4 files as </p> <p>mm10.fa.amb mm10.fa.ann mm10.fa.bwt mm10.fq.pac</p> <p>I read a thread that a guy's <a href='http://bio-bwa.sourceforge.net/'>BWA</a> …
-
How To Know The Progress Of Program Running Like Bwa Index Or Aln?
written by Tonyzeng •<p>Thank you for your answer, my question is that how to know progress of <a href='http://bio-bwa.sourceforge.net/'>BWA</a> index or aln when It is running under linux.</p>
-
About Mouse Reference Genome
written by Tonyzeng •<p>I have a question here, when I download mouse reference genome, this package has chr<em>.fa, *Un</em>.fa, <em>Hap</em>.fa and <em>random</em>.fa in it. before I concatenate them …
-
Questions About Pair-End Reads Which Are Not Match For Bwa
written by Tonyzeng •<p>My question is that my original data or pair end read data are consisted of Read1 and Read2 and they are corresponding to each other. …
-
Bwa Alignment Failed
written by Tonyzeng •<p>When I use new version <a href='http://bio-bwa.sourceforge.net/'>BWA</a> 0.7.5a to align my 78bp pair-end reads with reference genome under Linux, Index the genome and generate alignments …
-
Bwa Installation Failed After "Make" Command In Linux
written by Tonyzeng •<p>I am the first to install <a href='http://bio-bwa.sourceforge.net/'>BWA</a> and never use this software by commands of Linux.When I try to install <a href='http://bio-bwa.sourceforge.net/'>BWA</a> under <a …
-
Clarification For Running Bwa In Parallel
written by Mohamed •<p>Hi,</p> <p>I tried running <a href='http://bio-bwa.sourceforge.net/'>BWA</a> in parallel by splitting the input FASTQ file into 'n' splits and ran single ended alignment (aln and samse …
see that thread on SE: http://seqanswers.com/forums/showthread.php?t=6854&highlight=large+sample+calls
Pierre has been too gentle. I would suggest that you first use the search function here looking for "duplicates" or for "markduplicates", and also to use the "tags" section selecting any of those 2 mentioned tags. you'll find plenty of information there that describes what NGS duplicates are, why we have to consider them specially in the analysis, when it's advisable to remove them and when it's not,...