Questions tagged [dna-sequencing]

Technique(s) by which the sequence of DNA is obtained. The principles are similar for RNA-sequencing.

DNA sequencing is a group of techniques that are used to obtain the sequence of nucleotides in . When DNA sequencing is done for the entire genome of an organism then it is called genome-sequencing.

There are two main methodological principles for DNA sequencing:

  • Sequencing by termination: Sanger sequencing
  • Sequencing by synthesis: Most next generation sequencing methods

Sanger sequencing depends on termination of PCR reaction at different positions of a nucleotide. PCR termination happens because of the incorporation of a non-extensible di-deoxy-nucleotide (it lacks 3' OH; the triphosphate form is abbreviated as ddNTP), instead of a usual deoxy-nucleotide. This leads to formation of multiple products which indicate the location of a nucleotide in the DNA.

Sequencing by synthesis involves recording the nucleotide as it is inserted in the growing DNA.

Refer to the Wikipedia page on DNA sequencing for basic details.

Next generation sequencing (NGS) methods use a high level of automation that enables large scale sequencing. Refer to this review for more details on NGS.

Applications and variants of DNA sequencing:

  • ChIP-seq: Chromatin Immunoprecipitation followed by DNA sequencing (ChIP-seq) is used to identify regions of DNA that is bound by a certain protein, which in most cases is a transcription factor.
  • Nucleosome sequencing: Sequencing the regions bound the nucleosome; used to study chromatin architecture
  • Bisulphite sequencing: Bisulphite to deaminate methylated cytosine to thymine. This when compared to untreated DNA sequence, reveals sites of cytosine methylation.
  • MeDIP-seq: Methylated-DNA immunoprecipitation followed by sequencing: Also used to find methylated regions of DNA but uses an antibody to precipitate methylated DNA (cytosine).
  • DNAse Hypersensitive region mapping: DNA is treated with DNAse to identify regions protected by protein binding. Used for studying chromatin architecture
  • HiC: Genome level implementation of chromosome conformation capture (3C). Used for studying DNA-DNA interactions.

Questions that can have this tag:

  • Questions related to principle behind the sequencing techniques
  • Questions related to principle behind any of the above mentioned implementations of DNA sequencing
  • Questions related to experimental troubleshooting for any of these techniques
  • Questions related to analysis of sequencing data

Related tags are , and .

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Why are there N's after Sanger sequencing?

After sending a DNA sample for sequencing, the resulting sequence had N's in the beginning and end of the sequence. I know the N's mean that the computer can't tell what the base pair is, but why is this?
Kirby
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Finding proteins in DNA sequence

I have to do a task for a university task and I need to understand some things before figuring out how to do it. The task is the following: Find matches of known proteins (DNA-PolyI,II,III) to the specific E.Coli DNA, sequence. I downloaded in…
atmosx
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Alternate genetic codes in newly sequenced organisms

Variations of the standard genetic code are pretty rare, but as the cost of high-throughput genome sequencing continues to drop, there is a greater possibility of discovering additional exceptions. That being said, there is a clear emphasis in…
Daniel Standage
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How are whole Haplotypes for Sequencing isolated?

Is it possible to reliably isolate and amplify DNA from individual sperm and/or eggs (from a fish)? I'd imagine that the small amount of DNA would make the PCR a bit wacky. We've considered irradiating sperm and attempting to create haploid females…
kieran
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Is Sanger sequencing still used in labs, and therefore worth learning?

If iI were to have access to funds for research, would learning this technique be a boon for me? Or are next-gen sequencing methods all the range now? My knowledge of both are limited.
Ro Siv
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Why doesn't Sanger (fluorescent) DNA sequencing double count nucleotides?

My understanding is that PCR is carried out until a fluorescent nucleotide halts replication. The segments of DNA are fed through the capillary tube based on size, sifting through the segments from smallest to largest; subsequently, the sequence is…
Alzeon
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Sequencing rtPCR product

So I have a validated set of primers for rtPCR from Biorad that contains SYBR green. If I do rtPCR, can I use the rtPCR product after purifying it with a Qiagen PCR purification kit? Also, I'm under the impression that the sequencing company needs…
GPI
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What does it exactly mean to sequence the genome of a species?

Since all organisms are different from each other - that is, we all have different alleles, some SNP, microsatellites, etc. -, what does it exactly mean, for the genome of a species, to be sequenced? I understand what it means for an organism's…
michaelg
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Determining the Accuracy of DNA Testing

The DNA Testing firm in the below article claims that its tests were "99.99 per cent" accurate. http://www.telegraph.co.uk/news/uknews/1322077/False-DNA-test-led-father-to-reject-daughter.html Googling "dna test accuracy" has led to numerous…
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Is there a database containing sequences of human cell lines?

I'm looking for the whole genome sequences of several human cell lines, e.g., A549 or Ea.hy.926. Is there a database specifically dedicated to human cell lines?
Eekhoorn
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How much variation in the human genome for humans

We are currently learning about the Human Genome Project in high school biology. Wouldn't the human genome that was mapped be different from, say, mine if it was mapped? How much variation is there between individual humans in our genetic…
Sarah
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Understanding the strategy of Sanger DNA sequencing

The Sanger sequencing method creates large numbers of sequences of all possible lengths, ending with a specific nucleotide, by terminating with a tagged (fluorescent) nucleotide at the end. But if you already have fluorescent nucleotides of a…
user9807
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Why does low sequence diversity cause sequencing problems

When sequencers are processing sequence fragments, if there is little diversity at a particular bp locus this can cause problems for the sequencer. I have the superficial understanding that when a flow cell contains a significant percentage of a…
The Nightman
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Multiple clones Sanger sequencing analysis

I am doing a 96-well arrayed cloning. I have done Gibson, transformations and minipreps in a 96-well format, then sent out the plate for sequencing. Normally, I sequence 3-4 clones and check if the sequencing looks good manually with Benchling cause…
khorms
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How are fragments isolated during shotgun Sanger sequencing?

For a large genome (say millions of base pairs) -- we split the genome into fragments < 1000bp that are sequenced and can then be put back together computationally. My understanding is you use some sort of shearing technique to get the DNA into…
user491880
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