🎉✨ Great news! 🎉✨ ClevaLab has reached over 300,000 views on YouTube. 🚀 A huge thank you to everyone who's watched the videos. Let's learn biology together. 🤗
Watch our Channel. 🔗 https://t.co/XnnjafZQzD
#learnbiology#clevalab#molecularbiology#cellbiology
Why Use Sanger Sequencing When There's NGS? 🤔🧬 sequencing. Let's dive into the key differences in this video!
Check out the link for the full Sanger Sequencing video. 🔗 https://t.co/Gt9DCpLNqf
#SangerSequencing#learnbiology#ClevaLab#scicom#sequencing#scied
Unlock the secrets of dNTP and ddNTP naming and structure! 🤓 Understanding these building blocks is essential in the world of Sequencing. Check out the link to see the full video on Sanger Sequencing.
🔗 https://t.co/Gt9DCpLNqf
#dntp#genomics#sequencing#sangersequencing
Exciting news! Our latest blog post is up! 💻️ Head over to our Blog and check out "Sanger Sequencing, From Then to Now". Learn about the important #DNA#sequencing technique in #genetics.🤓
🔗 Follow the Link: https://t.co/2GG4av4h1v
#ClevaLab#scicomm
New video alert! 🎥 #ClevaLab just released our latest video on Sanger DNA #Sequencing! 🧬 This video breaks down the ins and outs of #SangerSequencing. Learn about the technique's history and innovations. Watch now on our YouTube channel! 🤓
#Genetics 🔗 https://t.co/Gt9DCpLNqf
Aligning and Making Sense of the NGS Reads. 🤓
Sequenced reads get mapped to the reference genome.
Follow the link for the full NGS video. 🔗 https://t.co/NKpz0bbcup
#genomics#dnasequencing#scicomm#science
Filtering Out the Low-Quality NGS Reads. 🤓
Low-quality reads include the clusters that overlap, lead or lag with sequencing or are of low intensity.
Follow the link for the full NGS video. 🔗 https://t.co/NKpz0bbcup
#genoimcs#ngs#science#biology
Sequencing the #DNA to Create Reads. 🧬
The #sequencing primer binds to the forward strands. Next, the complementary base binds to the sequence. Then the camera reads and records the colour of each cluster.
Watch the full NGS video: 🔗 https://t.co/NKpz0bbcup
#scicomm#genomics
The First Step of NGS. Attaching the Library to the Flow Cell. 🤓
Watch the full NGS video here: https://t.co/NKpz0bbcup
#sequencing#dnssequencing#genomics
How are DNA Libraries made for NGS? 🧬
Libraries get made by cutting the DNA into short pieces of a specific size. Then sequences of DNA called adapters get added to each end of a DNA fragment.
Watch the full NGS video here: https://t.co/NKpz0bbcup
#genomics#sequencing#ngs
Quality DNA is Important for #NGS. 🧬 #DNA and #RNA can be extracted from different samples and purified by column purification using a centrifuge. Then, the quality of the DNA or RNA is checked with a Nanodrop and TapeStation.
Watch the full video 🔗 https://t.co/NKpz0bbcup
The Human Genome Project took 32 years to complete all 3.2 billion bases of the human genome. Now with Next Generation Sequencing, a genome can be sequenced in one day.
Watch the full video on NGS here: https://t.co/NKpz0bbcup
#ngs#genetics#scicomm
A new video is out now on Next Generation Sequencing. 🤓Learn how NGS works, including library preparation, cluster generation, the sequencing reaction and filtering and alignment of sequencing reads.
Watch the video here: https://t.co/NKpz0bbcup
#sequencing#ngs#sequencingdna