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Overview of Illumina Sequencing by Synthesis Workflow | Standard SBS chemistry

Illumina

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Assumes interest and some biology. Education, not medical advice.

2.7M views10 years ago1 recommendation

How the body worksGenetics and genomicsCells and molecules

An animated overview of Illumina's next-generation sequencing workflow, demonstrating the process of sequencing by synthesis in 3D detail.

Explore the Illumina next-generation sequencing workflow, including sequencing by synthesis (SBS) technology, in 3-dimensional detail. Go from sample preparation, to cluster generation, to sequencing on a system flow cell with the proprietary SBS process, through to data analysis on the BaseSpace Sequence Hub. #Illumina #sequencingbysynthesis #nextgensequencing Please view our 2025 video, showcasing Illumina's newer chemistry (XLEAP SBS chemistry) here: youtu.be/EDVKxSNdSic For more information on the applications and advantages of SBS technology, visit illumina.com/technology/next-generation-sequencing/sequencin…

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1 person recommends this

What people say. Recommended as an excellent visual explanation of how modern DNA sequencing technology works.

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On “No human genome has ever been completely sequenced”

link to this video is the best visualization of how the most popular type of DNA sequencer works (that I've found). Imagine you have a string of length 3 billion made by randomly choosing from 4 characters. Like this dna = ''.join(random.choices('atgc', weights=30.9, 29.4, 19.9, 19.8, k=3_234_830_000)) you get to randomly sample 1 billion3, page 7 overlapping substrings of length 2003, page 7 with .1% of the characters randomly changed3, page 8. Trying to find the original string from this is technically an undecidable problem. If there's a sequence 400 characters long that repeats multiple times, how could you know if it repeats 5 times or 50 times? (this would be unlikely to happen with rando…

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On “Genomics – A programmer’s guide”

…on sequencing technologies: 1) short read - Illumina - dominates most next-generation sequencing 2) long read - nanopore or pacbio. These have very different analysis methods, have measurement errors that are very different, and even have different file formats, etc. Short read is far more common, so you're probably in the "Data Analysis" of this: link to this video But you need to know about the adapters and indices (how multiple samples can be sequenced at the same time). But as another commenter mentions, knowing some particulars about the project would really help know what sort of tutorial would be appropriate. You'll need to also know about the biology of the application, in addition to understan…

lkirkin Hacker News • Mentions

On “DNA Data Storage: The Entirety of YouTube Could Fit on a Teaspoon”

A sequencing run (at least in the context of Illumina's technology) requires a few very expensive consumable reagents: First being the flowcell (microscope slide that the dna sticks to while being read by a laser), the reagents (containing enzymes with fluorophores and other reagents for amplifying and manipulating DNA), and the actual power consumed by such machinery. This does not factor in prep/lab costs (which can be kept at a minimum with automation, but that also is a high startup cost endeavor). Each sequencing run can take ~1-3 days depending on the format. Edit: this video may be able to explain a little better how this process works: link to this video