my FastQC report shows sequence length as 20-36.Can I accept the sequence?
Basic Statistics...
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I ran FastQC software on RNA-Seq data of Plant sample generated from illumina HiSeq pla...
I am quality checking a gene sequence using FASTQC.
It has given me warnings about the sequence ...
I do a FastQC for quality control my data but i some situation there are a caution, can anyone te...
I am working on the genomic data of E. Coli. My sequence reads are of high quality, and I already...
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I have some Illumina RNA seq data, 75bp paired end reads. I've run FastQC & trimmomatic a...
I am trying to find bcftools consensus using GRCH38. But I am getting the following error. What d...
I have 32 fastq data from whole exome sequencing. I ran FastQC on them, and the following 3 items...
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I am having a ot of MiSeq data I am trying to analyze and I figured out using FastQ...
I have 50% duplicates on WGS on tumour samples and while I was expecting that the coverage will b...
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I have to analyze differential expression on 2 SRA files containing data from a small RN...
Dear all,
"TO TRIM OR NOT TO TRIM?"
My PE RNAseq library prep of human brain tissue was made wi...
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I am downloading public data, and am running FastQC on a number of FASTQ files I've downl...
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I am running tophat over reads with length equal to 36 to 38. And while running it the bel...
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I ran FastQC software on whole genome sequence (WGS) data of Human sample (with expected...
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I wonder if any body tell me about Per tile sequence quality?
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I am processing a ChIP-seq experiment I downloaded from GEO (link). The SRA files are mas...
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After using Illumina and de novo assembly on 23 bacterial genomes, I have used Mauve to re...
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After my training with Genemark, there are two kinds of warning in the "log" out...
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I have a large set of FASTQ files from genomic DNA. I ran them through FastQC and...
Hello! I'm quite new to NGS data analysis and have a few questions about certain modules in FASTQ...