Episodios

  • SE5: NGS in Immunology
    Aug 6 2025

    The science of white blood cells, and much more


    Chapters:

    05:30 Immunology how?

    22:05 22q11.2 deletion syndrome

    34:30 Scientific collaboration

    40:00 Data losses

    50:00 Flip it!

    53:00 outlook 2030


    Links:

    mini-immunology intro:

    https://www.youtube.com/watch?v=k9QAyP3bYmc



    22Q e. V. - zentraler Anlaufpunkt für Menschen mit Deletionssyndrom 22q11 oder Duplikationssyndrom 22q11 im deutschsprachigen Raum https://www.wirsind22q.de/aus-dem-verein/vorstand


    Podcast for young immunologists from young immunologists https://theyoungimmunologist.buzzsprout.com/


    Contact Nora here https://www.linkedin.com/in/nora-balzer-phd-253a767b


    Some information about training courses and events https://www.immunology.org/traininghttps://dgfi.org/dgfi-en/academy-of-immunology/


    Since 2018, West German Genome Center (⁠https://wggc.de/⁠) operates as the next generation sequencing facility and supports research in genomics & transcriptomics by providing expertise and sequencing services. WGGC is a part of the Next Generation Sequencing Competence Network (NGS-CN: ⁠https://ngs-kn.de/⁠) – network of NGS core facilities in Germany. Listen to our podcast and we're happy to receive your feedback&questions via Email (podcast[dot]explain[at]gmail[dot]com ).

    License Notice

    This podcast including all episodes, unless otherwise noted, is licensed under a ⁠⁠⁠⁠⁠Creative Commons Attribution 4.0 International License⁠⁠⁠⁠⁠.You are free to share, remix, and use this content as long as you give appropriate credit, provide a link to the license, and indicate if changes were made.

    Attribution:

    Podcast Title: Explain Podcast

    Creators: Iuliia Novoselova, Daniel Rickert

    Website: ⁠⁠⁠⁠⁠https://ngs-cn.de/explain-podcast/⁠

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    57 m
  • E15: Singular Genomics | ATAC-seq
    May 28 2025

    Sharing a flowcell, reinvented


    Chapters:

    - 00:00 usegalaxy.org

    - 07:55 Singular Genomics start

    - 21:55 Max Reads

    - 29:40 DNA Structure / ATAC-seq


    Setup galaxy on local hardware:

    https://galaxyproject.org/admin/get-galaxy/


    G4 is competing with Illumina:

    https://www.genengnews.com/topics/omics/fast-and-flexible-singulars-g4-takes-aim-at-illuminas-sequencing-superiority/


    Singulars chemistry is one of many:

    https://www.nature.com/articles/d41586-023-00512-4


    How max reads works:

    https://techwriting.singulargenomics.com/max-read/Max-Read-Kit-User-Guide-600026.pdf


    Small intro to DNA Structures:

    https://en.wikipedia.org/wiki/Nucleic_acid_quaternary_structure


    Intro to ATAC-seq:

    https://www.nature.com/articles/s41596-022-00692-9


    PS:

    As of 2025, Singular does not advertise DNA/RNA Sequencing on their G4 anymore, but shifted to spatial data, including their G4X: https://www.singulargenomics.com/



    Since 2018, West German Genome Center (⁠https://wggc.de/⁠) operates as the next generation sequencing facility and supports research in genomics & transcriptomics by providing expertise and sequencing services. WGGC is a part of the Next Generation Sequencing Competence Network (NGS-CN: ⁠https://ngs-kn.de/⁠) – network of NGS core facilities in Germany. Listen to our podcast and we're happy to receive your feedback&questions via Email (podcast[dot]explain[at]gmail[dot]com ).

    License Notice

    This podcast including all episodes, unless otherwise noted, is licensed under a ⁠⁠⁠⁠⁠Creative Commons Attribution 4.0 International License⁠⁠⁠⁠⁠.You are free to share, remix, and use this content as long as you give appropriate credit, provide a link to the license, and indicate if changes were made.

    Attribution:

    Podcast Title: Explain Podcast

    Creators: Iuliia Novoselova, Daniel Rickert

    Website: ⁠⁠⁠⁠⁠https://ngs-cn.de/explain-podcast/⁠

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    46 m
  • E14: Ultima Genomics + Element UltraQ
    Apr 2 2025

    Spinnin' bases on wafers to do mostly natural SBS


    Chapters:

    - 00:00 Ultima ePCR with beads

    - 07:10 Spinning the wafer, nucleotides, no blocking

    - 14:30 Ultima ppmSeq + Element UltraQ

    - 25:30 How Element UltraQ was born

    - 30:30 snakemake, cromwell, nextflow

    - 36:50 ncRNA


    Ultimas homepage: https://www.ultimagenomics.com/


    Nature paper with the chemistry: https://www.nature.com/articles/s41587-022-01452-6


    Elements UltraQ chemistry:

    https://www.elementbiosciences.com/cloudbreak-ultraq-enhanced-sequencing-accuracy-when-precision-matters-most


    Snakemake: https://snakemake.readthedocs.io/en/stable/


    Nextflow: https://www.nextflow.io/docs/latest/index.html


    Cromwell: https://cromwell.readthedocs.io/en/stable/


    Small overview of not all ncRNA types: https://microbenotes.com/types-of-rna/


    Since 2018, West German Genome Center (https://wggc.de/) operates as the next generation sequencing facility and supports research in genomics & transcriptomics by providing expertise and sequencing services. WGGC is a part of the Next Generation Sequencing Competence Network (NGS-CN: https://ngs-kn.de/) – network of NGS core facilities in Germany. Listen to our podcast and we're happy to receive your feedback&questions via Email (podcast[dot]explain[at]gmail[dot]com ).

    License Notice

    This podcast including all episodes, unless otherwise noted, is licensed under a ⁠⁠⁠⁠Creative Commons Attribution 4.0 International License⁠⁠⁠⁠.You are free to share, remix, and use this content as long as you give appropriate credit, provide a link to the license, and indicate if changes were made.

    Attribution:

    Podcast Title: Explain Podcast

    Creators: Iuliia Novoselova, Daniel Rickert

    Website: ⁠⁠⁠⁠https://ngs-cn.de/explain-podcast/⁠

    Más Menos
    46 m
  • E13: Sequencing by Avidity | Element Biosciences + XLEAP
    Mar 12 2025

    Because sometimes a jellyfish prevents quenching


    Chapters:


    01:00 - XLeap update from Illumina

    08:00 - Avidites start, splitting the problems

    13:20 - In-depth comparison to Illumina

    22:00 - Element summary

    23:30 - Bioinformatics tools: Jellyfish, KAT

    25:00 - QuickGen: GWAS


    Illumina about their XLeap: https://www.illumina.com/science/genomics-research/articles/data-quality-q-scores.html

    Sandiegomics about element: https://sandiegomics.com/element-beats-illumina-to-the-200-genome/


    Nature paper about the chemistry: https://www.nature.com/articles/s41587-023-01750-7


    Jellyfish for k-mer counting: https://github.com/gmarcais/Jellyfish


    GWAS Catalog: very nice data collection: https://www.ebi.ac.uk/gwas/diagram


    Correcting population-based GWAS bias: https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1011242



    Since 2018, West German Genome Center (https://wggc.de/) operates as the next generation sequencing facility and supports research in genomics & transcriptomics by providing expertise and sequencing services. WGGC is a part of the Next Generation Sequencing Competence Network (NGS-CN: https://ngs-kn.de/) - network of NGS core facilities in Germany. Listen to our podcast and we're happy to receive your feedback&questions via Email (podcast[dot]explain[at]gmail[dot]com ).

    License Notice

    This podcast including all episodes, unless otherwise noted, is licensed under a ⁠⁠⁠⁠Creative Commons Attribution 4.0 International License⁠⁠⁠⁠.You are free to share, remix, and use this content as long as you give appropriate credit, provide a link to the license, and indicate if changes were made.

    Attribution:

    Podcast Title: Explain Podcast

    Creators: Iuliia Novoselova, Daniel Rickert

    Website: ⁠⁠⁠⁠https://ngs-cn.de/explain-podcast/⁠

    Más Menos
    40 m
  • E12: PacBio ONSO | Sequencing by binding
    Jan 28 2025

    Because only one type of nucleotide is not complicated enough


    Chapters:

    01:35 Introducing old problems

    15:30 More Phred, more better

    34:40 QuickGen: genetic testing

    47:40 Bioinformatics tools: samtools


    PacBio ONSO Specs: https://www.pacb.com/wp-content/uploads/Onso-specification-sheet.pdf


    SBB explained by PacBio: https://www.pacb.com/blog/sbb-sequencing/


    Why higher quality is better: https://pmc.ncbi.nlm.nih.gov/articles/PMC11331594/


    Short read sequencing market heating up: https://www.nature.com/articles/s41587-022-01632-4


    SBB for visual learners: https://www.youtube.com/watch?v=i_mSaNBOVmQ


    Since 2018, West German Genome Center (https://wggc.de/)operates as the next generation sequencing facility and supports research in genomics & transcriptomics by providing expertise and sequencing services. WGGC is a part of the Next Generation Sequencing Competence Network (NGS-CN: https://ngs-kn.de/) - network of NGS core facilities in Germany. Listen to our podcast and we're happy to receive your feedback&questions via Email (podcast[dot]explain[at]gmail[dot]com ).

    License Notice

    This podcast including all episodes, unless otherwise noted, is licensed under a ⁠⁠⁠⁠Creative Commons Attribution 4.0 International License⁠⁠⁠⁠.You are free to share, remix, and use this content as long as you give appropriate credit, provide a link to the license, and indicate if changes were made.

    Attribution:

    Podcast Title: Explain Podcast

    Creators: Iuliia Novoselova, Daniel Rickert

    Website: ⁠⁠⁠⁠https://ngs-cn.de/explain-podcast/⁠

    Más Menos
    55 m
  • SE4: Long vs Short reads
    Aug 1 2024

    Mixing up long and cheap


    Chapters:

    00:00:00 Intro

    00:03:30 Florians history

    00:13:50 Q&A Ressources for Bioinformatics

    00:27:00 Long-read-tools.org

    00:35:42 ONT || PacBio

    00:57:00 Storage

    01:09:00 Outro


    Up-to-date, raw prices:https://albertvilella.substack.com/p/march-2024-ngsspecs-update


    Dovetail comparing the two long-read technologies:https://dovetailbiopartners.com/2023/08/10/pacbio-vs-nanopore-unraveling-the-sequencing-odyssey-in-life-sciences/


    Comparing PacBios old CLRs to ONT:https://academic.oup.com/g3journal/article/12/11/jkac192/6651842?login=true


    RNA Performance comparison, wonderful read:https://www.biorxiv.org/content/10.1101/2023.07.25.550582v1.full.pdf+html


    Integras 0.02$:https://www.integra-biosciences.com/united-states/en/blog/article/short-read-vs-long-read-sequencing


    Since 2018, West German Genome Center (https://wggc.de/) operates as the next generation sequencing facility and supports research in genomics & transcriptomics by providing expertise and sequencing services. WGGC is a part of the Next Generation Sequencing Competence Network (NGS-CN: https://ngs-kn.de/) - network of NGS core facilities in Germany. Listen to our podcast and we're happy to receive your feedback&questions via Email (podcast[dot]explain[at]gmail[dot]com ).

    Our podcast is an outreach activity within the national genomics facility "West German Genome Center" funded by the DFG (https://www.dfg.de/) (No. 407493903)

    License Notice

    This podcast including all episodes, unless otherwise noted, is licensed under a ⁠⁠⁠Creative Commons Attribution 4.0 International License⁠⁠⁠.You are free to share, remix, and use this content as long as you give appropriate credit, provide a link to the license, and indicate if changes were made.

    Attribution:

    Podcast Title: Explain Podcast

    Creators: Iuliia Novoselova, Daniel Rickert

    Website: ⁠⁠⁠https://ngs-cn.de/explain-podcast/⁠

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    1 h y 12 m
  • E11: MGI DNA Nanoball sequencing
    Jul 2 2024

    Rolling in circles to make DNA yarns


    Chapters:

    00:00 Bioinformatics Upper Crust Tools

    04:04 STAR

    05:00 MGI

    15:00 Daniels first contact

    20:00 Brief Market Overview

    22:30 Short read market

    26:00 DFG High Costs Sequencing Projects Application

    29:20 QuickGen: Introns and Exons

    35:00 Conclusion


    MGI vs Illumina: https://alitheagenomics.com/blog/how-do-rna-seq-results-compare-between-illumina-and-mgi-sequencing-platforms


    Rolling the circle: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568012/pdf/nihms894568.pdf


    MGI vs Illumina legal case:https://www.reuters.com/technology/illumina-ordered-pay-chinese-company-333-million-gene-sequencing-patent-case-2022-05-06/


    The basics of MGIs technology: https://www.youtube.com/watch?v=gThcHHh4R0w


    DFG Application:https://www.dfg.de/de/aktuelles/neuigkeiten-themen/info-wissenschaft/2024/ifw-24-30


    GTL/WGGC: https://www.gtl.hhu.de/wggc


    TSM link http://tsm.gtl.hhu.de/- submit your request and our colleagues will contact you


    Since 2018, West German Genome Center https://wggc.de/) operates as the next generation sequencing facility and supports research in genomics & transcriptomics by providing expertise and sequencing services. WGGC is a part of the Next Generation Sequencing Competence Network (NGS-CN: https://ngs-kn.de/) - network of NGS core facilities in Germany.

    Listen to our podcast and we're happy to receive yourfeedback&questions via Email ( podcast[dot]explain[at]gmail[dot]com ).

    Our podcast is an outreach activity within the national genomics facility "West German Genome Center" funded by the DFG (https://www.dfg.de/) (No. 407493903)

    License Notice

    This podcast including all episodes, unless otherwise noted, is licensed under a ⁠⁠⁠Creative Commons Attribution 4.0 International License⁠⁠⁠.You are free to share, remix, and use this content as long as you give appropriate credit, provide a link to the license, and indicate if changes were made.

    Attribution:

    Podcast Title: Explain Podcast

    Creators: Iuliia Novoselova, Daniel Rickert

    Website: ⁠⁠⁠https://ngs-cn.de/explain-podcast/⁠

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    37 m
  • E10: Genome Mapping
    May 27 2024

    Who needs all bases anyway?


    Chapters:

    00:00 Phasing

    08:50 Not Sequencing, really

    14:00 Bionano Saphyr Chip

    26:00 Nabsys - going electric

    29:30 Tools available

    39:00 QuickGen with Iuliia: Transposons!


    Links:

    Small explainer by CAP: https://www.cap.org/member-resources/articles/optical-genome-mapping-a-tool-with-significant-potential-from-discovery-to-diagnostics


    What genome mapping can be used for: https://www.mdpi.com/2073-4425/12/3/398


    Finding SVs with genome mapping: https://www.nature.com/articles/s41408-024-01059-x


    Bionano github repos: https://github.com/search?q=bionano&type=repositories&s=updated&o=desc

    Listen to our podcast and send your feedback to podcast[dot]explain[at]gmail[dot]com


    Since 2019, West German Genome Center https://wggc.de/ operates as the nextgeneration sequencing facility and supports research in genomics & transcriptomics by providing expertise and sequencing services. WGGC is a part of the Next Generation Sequencing Competence Network NGS-CN https://ngs-cn.de/ – network of NGS core facilities in Germany.


    The Explain Podcast is recorded at the Multimediazentrum at Heinrich-Heine University ofDüsseldorf https://www.mmz.hhu.de/ Our podcast is an outreach activity within the national genomics facility ”West German Genome Center” funded by the Ministerium für Kultur und Wissenschaft des Landes Nordrhein-Westfalen https://www.mkw.nrw/land-foerdert-spitzenzentrum-fuer-genomsequenzierung-nordrhein-westfalen/

    License Notice

    This podcast including all episodes, unless otherwise noted, is licensed under a ⁠⁠⁠Creative Commons Attribution 4.0 International License⁠⁠⁠.You are free to share, remix, and use this content as long as you give appropriate credit, provide a link to the license, and indicate if changes were made.

    Attribution:

    Podcast Title: Explain Podcast

    Creators: Iuliia Novoselova, Daniel Rickert

    Website: ⁠⁠⁠https://ngs-cn.de/explain-podcast/⁠

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    48 m