Ben Price

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Ben Price

Ben Price

@ento_ben

Curator of all the flies that aren't Flies @ the Natural History Museum, London 🌍 Instagram: benpricepix

London Tham gia Kasım 2012
883 Đang theo dõi828 Người theo dõi
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Rudolf Meier @rudolf-meier.bsky.soci
🚨 EntoSieve: New automated tool for fast, accurate size-sorting of bulk insect samples! Perfect for boosting DNA megabarcoding & metabarcoding projects. 🧬🔬 DIY low-cost device, gentle on specimens and yet efficient 🦋🐞read here: authorea.com/users/836612/a…
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Science at the Natural History Museum
OPPORTUNITY! We are recruiting an exceptional leader for NHM Collections: Director of Collections: You'll lead a dedicated team, spearhead strategy for the future of collections, drive access and research, and ensure success of our multi-site expansion nature.com/naturecareers/…
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Jan Macher
Jan Macher@JNMScience·
🚨 Job Alert! 🚨 Naturalis is hiring two tenure-track researchers. We're looking for experts who want to integrate molecular techniques, imaging, and data science (AI) to advance species recognition and detection. Apply here: naturalis.nl/en/about-us/jo…. #Biodiversity #metabarcoding
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Bento Lab 🧬
Bento Lab 🧬@theBentoLab·
If you want something super simple and reasonably priced, microCLEAN may be worth trying: microzone.co.uk/shop/post-ampl… (I would love to know how it works in terms of chemistry!). Or you could try a cheap magnetic bead cleanup with reagents and magnet rack, possibly cheapest and most accessible from sergilabsupplies.com/products/magne… haven’t tested these myself though). If you want something very inexpensive but more time consuming and have enough samples to warrant stocking up on PEG, salt, and ethanol, a PEG precipitation may be useful, e.g.: sites.lsa.umich.edu/olsen-lab/wp-c… . You could also try a freeze-and-squeeze extraction method extracting from TAE gels, e.g. x.com/theBentoLab/st… There will also be other methods, e.g. homemade spin columns, bought spin columns with homemade reagents, etc. The question of which method would work best for you will probably depend on your own preferred balance of cost/speed/scalability/yield/reliability! Hope that helps!
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DominikBuchner
DominikBuchner@buchner_dominik·
Just updated BOLDigger2: By popular demand 🫡, BOLDigger2 now accepts BOLD credentials as optional arguments for seamless integration into existing bioinformatics pipelines. Update now at github.com/DominikBuchner…! #boldigger2 #update 💻
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Kara Dicks
Kara Dicks@kara_dicks·
We’re sequencing the genomes of 10 endangered species with ORG.one live at London Calling! 🦁🦛🐛🐧🦆🐆🦌 Thanks to @NHM_London and @rzss for making this possible and helping to generate useful genomic data to support conservation efforts! #nanoporeconf
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Ben Price
Ben Price@ento_ben·
With >45,000 individual specimen barcodes generated in a single MinION run, sequencing is no longer the hard / expensive part of doing DNA based biomonitoring!
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Ben Price
Ben Price@ento_ben·
The samples were shipped to @SangerToL and non-destructively DNA extracted by @marakat’s team and @sangerinstitute Scientific Operations who then ran 92,160 PCRs (the protocol is a two step PCR carried out in 384-well plates).
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Ben Price
Ben Price@ento_ben·
These barcodes are from over 45,000 arthropod specimens held in 480 96-well plates, where each well contains a single specimen collected using Malaise traps by the wonderful partners participating in the @BIOSCAN_UK project led out of @SangerToL and @marakat’s group
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