Excited to see this work published. Lancet2 comes with many improvements in genotyping, variant scoring, visualization, and runtime. Outstanding work of @omicsnut. Great collab. with Benedict Paten group. Work supported by @theNCI under #NCIITCR. Article: https://t.co/iGNJR766mM
NEW: Hotels and motels have quietly become New York’s most common solution for emergency shelter for homeless people outside NYC.
Many stay in dilapidated rooms without the social services that shelters are required to provide.
https://t.co/YdEHZn2157
Grateful for the opportunity to present our CLONEVO investigator-initiated trial (IIT) in bladder cancer at @ASCO#ASCO2025. Here are some lessons I learned along the way:
Investigator-initiated trials (IITs) are essential. IITs are clinical trials independently designed and led by physician-scientists. These trials usually start from scientific observations in the lab. They are driven by unmet clinical needs, making them uniquely powerful for testing new therapeutic hypotheses!
Investigator-initiated trials are hard! Taking something from the laboratory to the bedside 🔬➡️ 🛏️ takes years of sustained effort.
It takes a team. This truly takes a huge team of brilliant and dedicated colleagues, including clinicians such as oncologists, pathologists, urologists, research nurses, laboratory scientists, computational biologists, regulatory staff, and many more! @MHosmanMD@cnsternberg@DoctorMargolis@DrJonesNauseef@DrAnaMolina@DrDavidNanus@rohitjainMD
@scientistatlrge @DrMhidalgo@notSoJunkDNA@willbfx@ElementoLab@SuzanneColeMD@scherr_doug #clinicaltrials #teamscience
🤝 This is a model of successful industry-academia collaboration. We made the initial discoveries @WeillCornell@FaltasLab designed and conducted the trial. @EliLillyandCo supported the trial, and @CarisLS supported whole-exome (WES), ctDNA WES, and RNAseq—and shared the raw data so we could do our deep computational analyses in-house and with our collaborators. We were supported by @WCM_MeyerCancer@nyphospital
🪟 The window-of-opportunity design is a powerful platform to directly test on-target 🎯 activity in vivo, understand how therapies affect disease biology, and measure the effect directly in clinical samples. In our study of #bladdercancer patients, we collected pre/post-treatment tissues, ctDNA, and urine cfDNA. We worked with @WCMEnglanderIPM to establish patient-derived organoids and xenografts and performed spatial imaging mass cytometry of 630,000 single cells.
💡 Encouraging to see an efficacy signal — and even better when we can understand the underlying biology at the same time!
🙏 Immense gratitude to the patients and families who made this possible. You inspire us every day.
Funding for science and cancer research is essential. Without it, we wouldn’t be able to do this work, to take new therapeutic ideas from bench to bedside and bring hope to patients with cancer. @ASCOPost@JCO_ASCO@OncoAlert@OncBrothers @medicalwatchBC
@PGrivasMDPhD@TwoOncDocs@OncBrothers@Larvol@TiansterZhang@GlopesMd@HammersMD@sonpavde@drenriquegrande@scserendipity1@BraunMDPhD@Uromigos@AminNassarMD@ZiadBakouny@DrRanaMcKay@NazliDizman@urotoday@Uromigos@DrChoueiri
Excited to share our exploration @naturemethods into new horizons opening up in the era of low cost sequencing!
🔥 Deeper sequencing at WGS scale for PPM sensitivity of tumor informed MRD
🔥Duplex sequencing at WGS scale for plasma only exploration of ctDNA
Check out thread 👇
🚀Big News! Excited to share our work “The Interplay of Mutagenesis and ecDNA Shapes Urothelial Cancer Evolution” published in @Nature! https://t.co/sU6uF9rNvI
Special nugget for my genomics friends in today's paper: Read everything but don't miss Extended Data Fig. 8, where @willbfx assembled a CCND1-ecDNA from @nanopore reads!
"Did you know that you don't need targeted panels for ultra-sensitive MRD?"
🥳 Down right ebullient to share our latest 🥳@NatureMedicine !
MRD-EDGE leverages advanced #ML for #WGS#ctDNA detection across clinical context
https://t.co/drJasWVwoE
#DeepLearning
🪡
Human cancer is a disease of somatic mutations. As we age, tissues accumulate errors in DNA, but what causes mutations in young healthy cells? Read our new paper “Childhood cancer mutagenesis caused by transposase-derived PGBD5” https://t.co/B3RKAtYIWd 1/n
We (@nygenome cancer compbio group) are very fortunate to work closely with @WCMEnglanderIPM and have several papers in preparation. Here is one focused on brain metastases in prostate cancer with @FKhaniPath@willbfx@mishabeltran
https://t.co/v7rT6XQV3v
Pre-print alert 🚨Excited to share our new preprint “The interplay between mutagenesis and extrachromosomal DNA shapes urothelial cancer evolution” 🧬🔬#bladdercancer https://t.co/lDZf36CpB9 @OncoAlert
NY Genome Center Team Harnesses Ultima Genomics Platform for High-Sensitivity ctDNA Sequencing. Taking advantage of the new platform’s low sequencing cost, the researchers sequenced cell-free circulating DNA (ccfDNA) in plasma at high depth for... https://t.co/EdHALvo6H5
🔥Extra-hot pre-print before this hellsite goes up in smoke 🔥
New horizons open up when sequencing costs go ↘️ @UltimaGenomics
Interested in deep cfDNA WGS for ultra-sensitive cancer detection? Duplex sequencing at genome scale?
https://t.co/DJeCo86ok8
Check out 🪡👇
Read our latest on the causes of oncogenic DNA rearrangements in medulloblastomas, a common childhood brain tumor: Childhood cancer mutagenesis caused by a domesticated DNA transposase https://t.co/4h37LJEoSv