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• Fastq Groomer
  Hi all, Fastq groomer has Solexa or Illumina 1.3+ as an input quality format. I asked at the seq...
• Question About Fastq Groomer
  To Whom It May Concern: I am a new user to Galaxy. In the function of "FASTQ Groomer", I notic...
• GROOMER ON NEXTSEQ500 DATA
  Dear community, I am a beginner....trying to use Trimmomatic to clean adaptors/index from my Nex...
• Fastq Groomer Processing Time
  I used FASTQ groomer on a 29 Gb Illumina 1.5+ FASTQ file to go from Illumina 1.3-1.7+ to Sanger a...
• Fastq To Fastqsanger Using Groomer Question
  Hello! I am fairly new to using Galaxy and have a question about the FASTQ Groom...
• Fastq Joiner Problem
  Hi, I am trying to join two groomed fastq files from a paired-end Illumina read using the fastq j...
• Fastq Sanger To Illumina Fastq
  I want to convert Sanger FASTq to Illumina FASTq with a understanding that Sanger is the current ...
• Question About Fastq Groomer
  Hi Jianchao, The different fastq formats are broadly summarised by: S - Sanger Phred+33...
• Fastq Splitter Produced Empty Dataset, Please Help
  I have problem to split a paired-end FASTQ dataset into two separate datasets. In order to explai...
• Transfer FASTQ data from external resource to Galaxy
  Dear all Please how can I transfer a FASTQ file directly from Illumina basespace to Galaxy? Thank...
• Have Fsatq ... But Don'T Know Input Format For Groomer?
  Hello, My account login is: johnsonko@ninds.nih.gov I am a first time Galaxy user. I have uplo...
• not select Fastq File
  I get data (Fastq File Illumina), but when I would like to use Fastq summary statistics (NGS>Q...
• Fastq Quality Trimmer For Pe Illumina?
  Hello, I was wondering, can Galaxy's FASTQ Quality Trimmer tool be used on Illumina paired-end d...
• Analysis of paired end illumina sequence.
  Hi everyone, I am  new in NGS.  I would like to filter and identify V4 region from raw paired en...
• Tools does not recognize input dataset: set proper datatype metadata
  My NGS files are fastq files but not recognized by Bowttie2 or Map with Bowtie for Illumina from ...
• Forward and Reverse reads from paired end sequencing
  The fastq dataset we have after illumina whole genome sequencing is in the form of two files - fo...
• Need help with "FASTQ Trimmer" tool
  FASTQ Trimmer seems unable to recognize my FASTQ files as input. For e.g. I carried out FASTQ to ...