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 02-20-2014, 04:24 AM #1 Neiltje Member   Location: Belgium Join Date: Jan 2014 Posts: 21 Miseq questions from a newbie Hi, I'm new in the sequencing world (apart from standard courses in university). I've prepared an RNAseq library using the Scriptseq protocol from Epicentre. Together with a co-worker we sequenced it on a V2 150bp (300 cycles) cassette. Now I'm learning more about sequencing, I'm wondering why we used this cassette and not another one. Next week, I'm going to prepare a library of small RNA's for sequencing. The fragment size will be around 147 bp (sequence itself + adaptor + indices). But my boss told me to order the v2 cartridge of 50 cycles. Now I'm wondering how long the reads will be that come out of it. If it is 2 x25bp, won't the Miseq read only the adaptor and never the sequences of interest itself? I'm sorry if these are really silly question, I'm just getting the hang of it.
 02-20-2014, 04:33 AM #2 Neiltje Member   Location: Belgium Join Date: Jan 2014 Posts: 21 Oh and another question. Why is sequencing of a PCR fragment on a Miseq overkill?
 02-20-2014, 04:38 AM #3 GenoMax Senior Member   Location: East Coast USA Join Date: Feb 2008 Posts: 7,015 Number of cycles is equal to number of bases you are going to get for each sequence read. So your 50 cycle single-end run will yield 50bp from (let us just say from left end) of a fragment. If you did a paired-end 50 cycle run then that will give you an additional 50 bp of sequence (from the right end) of the SAME fragment. So for a ~150 bp fragment Code: ``` DNA Fragment ---------------------------- Single-end (50 bp) ---------> <--------- Paired-end (50 bp)``` Sequencing PCR fragments is something people do all the time on MiSeq. It is a popular application for MiSeq.
 02-20-2014, 04:43 AM #4 Neiltje Member   Location: Belgium Join Date: Jan 2014 Posts: 21 So my thinking was right, 50 cycles for a fragment of +/- 147 bp, will not cover the sequence in the middle? 50 bp from the right and 50 bp from the left, still leaves 47 bp in the middle. About the PCR fragment: if you do primerdesign for the fragment you're interested in, you need to design primers compatible to your DNA + adaptor and index sequence(s). Aren't this really long primers?
 02-20-2014, 04:46 AM #5 GenoMax Senior Member   Location: East Coast USA Join Date: Feb 2008 Posts: 7,015 If you want the fragments to overlap in the middle then you will need to do a longer (100 bp) paired-end run (which may require a different kit). There is software available that can then stitch the reads together to form a single long read (MiSeq software can do this on the machine or you can use other programs like FLASH). Here are example threads for primer design: http://seqanswers.com/forums/showthread.php?t=20373 http://seqanswers.com/forums/showthread.php?t=33556 http://seqanswers.com/forums/showthread.php?t=17816 Last edited by GenoMax; 02-20-2014 at 04:48 AM.
 02-20-2014, 06:57 AM #6 microgirl123 Senior Member   Location: New England Join Date: Jun 2012 Posts: 199 "About the PCR fragment: if you do primerdesign for the fragment you're interested in, you need to design primers compatible to your DNA + adaptor and index sequence(s). Aren't this really long primers?" Yes but there are ways around it. You wouldn't want to sequence a single PCR amplicon on the MiSeq - it's appropriate for mixed amplicons such as mixed 16s sequences.
02-20-2014, 07:05 AM   #8
Neiltje
Member

Location: Belgium

Join Date: Jan 2014
Posts: 21

Quote:
Ok, thank you
I just discovered Illumina has a lot of online training video's. They also clarify a lot.