Yes the 100-900Bp fragment length limit is a problem. The first 100 are lost because they come off the TLC to fast everything above 900 tends to overlap. I have an internship this summer in which we are working on combining a fluorescence decay measurement with the normal florescence spectra so we can double up the readings and improve the accuracy and range of DNA sequencers.
The break through device I read of (in scientific American) is a single nm channel in which just one DNA strand goes through, as it goes it passes under a laser that somehow reads each nucleotide dye individually. So there is no need for PCR and fragmenting. All you need is a template (original) single DNA strand and specialized dye nucleotides to make the complimentary strand. Because the distance between nucleotides is about .5nm I don’t know how their going to get a laser beam thin enough to read each nucleotide separately?
The break through device I read of (in scientific American) is a single nm channel in which just one DNA strand goes through, as it goes it passes under a laser that somehow reads each nucleotide dye individually. So there is no need for PCR and fragmenting. All you need is a template (original) single DNA strand and specialized dye nucleotides to make the complimentary strand. Because the distance between nucleotides is about .5nm I don’t know how their going to get a laser beam thin enough to read each nucleotide separately?
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