
Raheleh Rahbari
@R_Rahbari
Followers
117
Following
63
Media
1
Statuses
29
Cancer Research UK Fellow | Group Leader the @Wellcome Sanger Institute. Interested in mutations acquired during aging and their impact across generation.
Wellcome Sanger intitute
Joined November 2024
RT @leeat_keren: 🚨Preprint Alert!🚨.Cell classification is one of the most difficult tasks in analyzing spatial data. We present CellTune -….
0
14
0
RT @genomeresearch: Call for Papers! @genomeresearch is now encouraging submissions for a Special Issue on The Genetics and Genomics of Som….
0
13
0
RT @naxerova: Interested in the mysteries surrounding metastasis evolution? . This perspective in @NatureRevCancer is my best attempt at pr….
0
43
0
RT @eventsWCS: Applications are closing on 1 April for our #EBECancer25 course⏰. Our expert trainers and speakers will guide you through ho….
0
3
0
RT @JohnTadross: 🚨 New paper in @Nature! 🚨.We’ve mapped the human hypothalamus in unprecedented detail, revealing key differences from mice….
0
77
0
RT @naxerova: Cancer evolution enthusiasts - you might be interested in some new data from our lab on quantifying cell divisions along evol….
0
73
0
RT @AndyRusss: Excited to share a short article I wrote describing: Slide-tags - which enables spatial single-nucleus sequencing, allowing….
0
7
0
And of course, we’re deeply grateful to the participants from @TwinsUKres , none of this would be possible without you. 🙏.
0
0
3
This study reflects years of dedicated work with an incredible team. Special shoutouts to @MDC_Neville for his outstanding work, @imartincorena, @mehurles, @kerrin_small, and all the amazing co-authors involved.
1
0
3
We made even more interesting findings! Take a look at @MDC_Neville’s tweetorial for a deeper dive:
Excited to share our new preprint in which we address:.(1) Accurate sequencing of sperm at scale.(2) Positive selection of spermatogenesis driver mutations across the exome.(3) Offspring disease risks from male reproductive aging.[1/15].
1
0
1
Using the latest NanoSeq method [, beautifully described by @imartincorena , we conducted deep exome NanoSeq. This allowed us to detect genes under selection in sperm.
Excited to share our latest work. We introduce an improved version of NanoSeq, a duplex sequencing protocol with <5 errors per billion bp in single DNA molecules, and use it to study the somatic mutation landscape of oral epithelium in >1000 people. 1/n
1
0
1
RT @doctor_msc: Stem cell transplants are amazing. A patient's diseased blood is replaced by a relative or stranger's. But what does puttin….
0
54
0
RT @RegevSchweiger: Our new preprint is up - “Insights into non-crossover recombination from long-read sperm sequencing”!. .
0
18
0