Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Assessment of Automated Flow Cytometry Data Analysis Tools within Cell and Gene Therapy Manufacturing
by
Braybrook, Julian
, Campbell, Jonathan J.
, Petzing, Jon
, Thomas, Robert J.
, Cheung, Melissa
in
Algorithms
/ Cluster Analysis
/ Data Analysis
/ Datasets
/ Flow Cytometry - methods
/ Genetic Therapy
/ Good Manufacturing Practice
/ Humans
/ Manufacturing
/ Medical equipment
/ Reproducibility of Results
/ Software
2022
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Assessment of Automated Flow Cytometry Data Analysis Tools within Cell and Gene Therapy Manufacturing
by
Braybrook, Julian
, Campbell, Jonathan J.
, Petzing, Jon
, Thomas, Robert J.
, Cheung, Melissa
in
Algorithms
/ Cluster Analysis
/ Data Analysis
/ Datasets
/ Flow Cytometry - methods
/ Genetic Therapy
/ Good Manufacturing Practice
/ Humans
/ Manufacturing
/ Medical equipment
/ Reproducibility of Results
/ Software
2022
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Assessment of Automated Flow Cytometry Data Analysis Tools within Cell and Gene Therapy Manufacturing
by
Braybrook, Julian
, Campbell, Jonathan J.
, Petzing, Jon
, Thomas, Robert J.
, Cheung, Melissa
in
Algorithms
/ Cluster Analysis
/ Data Analysis
/ Datasets
/ Flow Cytometry - methods
/ Genetic Therapy
/ Good Manufacturing Practice
/ Humans
/ Manufacturing
/ Medical equipment
/ Reproducibility of Results
/ Software
2022
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Assessment of Automated Flow Cytometry Data Analysis Tools within Cell and Gene Therapy Manufacturing
Journal Article
Assessment of Automated Flow Cytometry Data Analysis Tools within Cell and Gene Therapy Manufacturing
2022
Request Book From Autostore
and Choose the Collection Method
Overview
Flow cytometry is widely used within the manufacturing of cell and gene therapies to measure and characterise cells. Conventional manual data analysis relies heavily on operator judgement, presenting a major source of variation that can adversely impact the quality and predictive potential of therapies given to patients. Computational tools have the capacity to minimise operator variation and bias in flow cytometry data analysis; however, in many cases, confidence in these technologies has yet to be fully established mirrored by aspects of regulatory concern. Here, we employed synthetic flow cytometry datasets containing controlled population characteristics of separation, and normal/skew distributions to investigate the accuracy and reproducibility of six cell population identification tools, each of which implement different unsupervised clustering algorithms: Flock2, flowMeans, FlowSOM, PhenoGraph, SPADE3 and SWIFT (density-based, k-means, self-organising map, k-nearest neighbour, deterministic k-means, and model-based clustering, respectively). We found that outputs from software analysing the same reference synthetic dataset vary considerably and accuracy deteriorates as the cluster separation index falls below zero. Consequently, as clusters begin to merge, the flowMeans and Flock2 software platforms struggle to identify target clusters more than other platforms. Moreover, the presence of skewed cell populations resulted in poor performance from SWIFT, though FlowSOM, PhenoGraph and SPADE3 were relatively unaffected in comparison. These findings illustrate how novel flow cytometry synthetic datasets can be utilised to validate a range of automated cell identification methods, leading to enhanced confidence in the data quality of automated cell characterisations and enumerations.
Publisher
MDPI AG,MDPI
This website uses cookies to ensure you get the best experience on our website.