ecoli Posted November 19, 2005 Posted November 19, 2005 Does anybody have any good scientific/technical papers that explain this? I don't need actual papers, just references or links. I doing a sequencing reaction in my lab, but doing the assay and understanding what's going on are two different things. I'm trying to get a better grasp on what I'm doing. Thanks
rakuenso Posted November 19, 2005 Posted November 19, 2005 are you using the dideoxy method or shotgun method? and what kind of sequences are we talking about? Genomic? Plasmid? or etc...
ecoli Posted November 19, 2005 Author Posted November 19, 2005 dideoxy method, sequencing a plasmid. Sorry about the lack of detail.
rakuenso Posted November 19, 2005 Posted November 19, 2005 if its just simple dideoxy kimball has a nice explanation on it: http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/D/DNAsequencing.html
ecoli Posted November 19, 2005 Author Posted November 19, 2005 thanks rakuenso, thats a good paper. Any others? Do they get more technical, perhaps?
rakuenso Posted November 19, 2005 Posted November 19, 2005 http://www.nottingham.ac.uk/~mbzspd/methods/DNA_Sequencing.html Here's one that lists reagents and buffers
donkey Posted November 20, 2005 Posted November 20, 2005 are you using the dideoxy method or shotgun method?I'm a bit confused, couldn't (wouldn't?) the shotgun method use dideoxy sequencing (i.e. it's not either or). My vague understanding is that shotgun sequencing is essentially a method used for assembling sequences together in order to reconstruct sequences of large stretches of DNA (such as a genome) whereas dideoxy (Sanger) sequecing tells us which actual base pair molecules appear in order.
Yggdrasil Posted November 20, 2005 Posted November 20, 2005 Yes, the shotgun method is more of a method of assembling sequencs obtained from dideoxy sequencing into a full genome. An alternative to dideoxy sequencing is chemical sequencing which uses chemicals which degrade specific base pairs. First you label the 5' end of DNA with a 32P, then you would incubate the DNA with a low concentration of these chemicals for a specified time so that on average you have one clevage per DNA molecule. Electrophoresis of the fragments and visualization by autoradiography allows one to determne the sequence. Chemical sequencing methods are not widely used anymore because it's much easier to automate dideoxy sequencing. Also, using fluorescently tagged ddNTPs is preferable to using the radioisotopes and hazardous chemicals required in chemical methods.
BeYeu05 Posted February 28, 2006 Posted February 28, 2006 I Scholar Googled "DNA Sequencing" and landed upon the following page: http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/D/DNAsequencing.html
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