Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • jtotheulie
    Member
    • May 2016
    • 12

    #1

    Oxford Metrics

    Hi,

    I am starting a huge oxford project that will generate a huge amount of nanopore sequencing runs. I have yet to start but in my preparations I am making a log of what metrics I should record and also what constitutes a failing metric from a good metric (lowest passing metric and highest passing metric).

    Lib Prep:
    Initial DNA input (min = 1ug, max=?)
    Qubit read after Ampure
    Qubit read after Myone bead elution (min=200ng, max?)

    Sequencing:
    How many accessible pores
    Average read length
    Amount of 2D reads
    Amount of 1D reads
    Sequencing time

    Are there others?
    What are the top and bottom limits to each metric?
    Things to watch out for or pluggins to utilize while sequencing is happening?

    Thanks!!!!
  • ymc
    Senior Member
    • Mar 2010
    • 496

    #2
    Sorry to interject my question into your thread. I think it is somewhat relevant, so I hope you don't mind.

    Based on my analysis of nanopore fast5 I downloaded from ENA, I noticed there are two types of fast5 that has their 2D flag turned off: one with template events only and one with both template and complement events.

    I suppose they are all 1D reads. But what's the difference between the 1D read with both template and complement events and the true 2D reads? Is it that the latter comes from one molecule but the former comes from two different molecules?

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
      by SEQadmin2



      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

      Despite this, “CRISPR helped turn genome editing from a specialized technique into
      ...
      Today, 11:01 AM
    • SEQadmin2
      Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
      by SEQadmin2


      Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

      The systematic characterization of the human proteome has
      ...
      07-20-2026, 11:48 AM
    • SEQadmin2
      Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
      by SEQadmin2



      Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
      ...
      07-09-2026, 11:10 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Today, 02:55 AM
    0 responses
    7 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-24-2026, 12:17 PM
    0 responses
    11 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-23-2026, 11:41 AM
    0 responses
    12 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-20-2026, 11:10 AM
    0 responses
    24 views
    0 reactions
    Last Post SEQadmin2  
    Working...