Introducing AF-Pipeline, open-source Python package for extracting confident structures, interfaces from AlphaFold predictions https://t.co/tsxVTfXSaA
Github: https://t.co/CSytAkEdEZ. Designed and developed by @Omkar_Golatkar_ , initialized by @KartikMajila , tested by @muskaanjl
@rebeccaperrotto Your love for Liv is breathtaking. With deep respect, some families in palliative care have explored ketogenic metabolic therapy (Dr. Thomas Seyfried @tnseyfried) for comfort support and energy. Only something you might ask your care team about, if it ever feels right.
RUNX1C isoform identified as driver of chemoresistance in acute myeloid leukemia - ... a way to potentially disarm it. In findings newly published in Blood Cancer Discovery, a team led by JAX assistant professor Eric Wang reports on ... - https://t.co/M4VcGM5JN2
Happy to share our latest publication in Scientific Data @ScientificData on genome assembly and annotation of Nasonia oneida, the youngest species in the jewel wasp complex. @IiserMohali@DBS_IISERM
https://t.co/YwoWBWCafD
Postdoc position in our group at @emblebi , analyzing single cell data to better understand and treat neurodegen diseases, collab with @AndrewBassett43 , @mo_lotfollahi, @bayraktar_lab M Strauss and others @OpenTargets . Deadline 20/07.
Please share🙏: https://t.co/AkQCHMIevR
Thrilled to see #SAVANA out in @naturemethods🥳 SAVANA detects haplotype-resolved somatic SVs and copy number aberrations (SCNAs) and infers tumour purity & ploidy in clinical samples using long-read sequencing with or WITHOUT a matched germline control 👇https://t.co/AdZhqHUsDb
Deep-learning-based single-domain and multidomain protein structure prediction with D-I-TASSER @NatureBiotech
1.D-I-TASSER is a hybrid deep-learning and physics-based pipeline that outperforms AlphaFold2 and AlphaFold3 in both single-domain and multidomain protein structure prediction.
2.Unlike AlphaFold’s end-to-end deep learning, D-I-TASSER integrates multiple deep learning restraints (distance/contact/hydrogen-bonding) with fragment-based simulations, enabling superior structural refinement, especially for difficult targets.
3.For 500 nonredundant hard protein domains, D-I-TASSER achieved an average TM-score of 0.870 — 5% higher than AlphaFold2 and significantly higher than all other versions of AlphaFold, including v3.
4.On hard domains where AlphaFold2 struggled (TM < 0.8), D-I-TASSER showed a dramatic improvement (average TM = 0.707 vs. 0.598), successfully folding 63 cases where AlphaFold2 failed.
5.A key innovation is the domain-splitting and reassembly protocol, allowing D-I-TASSER to handle large multidomain proteins with better interdomain orientation than AlphaFold2.
6.On 230 multidomain proteins, D-I-TASSER achieved higher full-chain TM-scores in 88% of cases. The average TM-score improvement was 12.9% over AlphaFold2.
7.For large multidomain proteins (e.g. PDB 7jtkB, 6irdC), D-I-TASSER accurately modeled both interdomain and intradomain distances, where AlphaFold2 failed due to shallow MSAs.
8.DeepMSA2, the new iterative MSA generation module, is crucial to D-I-TASSER’s success. It builds deeper alignments and boosts model quality significantly, especially for orphan proteins.
9.In CASP15 blind tests, D-I-TASSER created correct folds for 95% of domains and outperformed AlphaFold2 and other top groups by a wide margin, particularly in interdomain modeling.
10.Unlike static AlphaFold predictions, D-I-TASSER produces diverse conformations, effectively capturing multiple states like open/closed forms in spike protein complexes.
11.D-I-TASSER was used to model over 95% of the human proteome, creating 34,968 domain-level and 19,512 full-chain structures. Many of these complement AlphaFold’s database coverage.
12.Estimated TM-score evaluations (eTM) indicate that D-I-TASSER’s models are robust, even in the absence of experimental structures, providing confidence for genome-scale structural annotation.
13.Overall, D-I-TASSER sets a new standard by combining deep learning with classical simulation, achieving high accuracy across difficult, large, and multidomain targets.
💻Code: https://t.co/jFgKsWmTiL
📜Paper: https://t.co/STmwJ6CeWl
#DeepLearning #ProteinStructure #StructuralBiology #AlphaFold #DITASSER #Bioinformatics #CASP15 #HumanProteome #Multidomain #MSA
💪 What if we could map muscle repair pixel by pixel?
🔬 Our group leader Dr @Wi_Roman (@ARMI_Labs) built a low-cost spatial transcriptomics platform to do just that - revealing how muscles heal, grow & communicate.
It's reshaping regenerative medicine.
https://t.co/jZ3jMEosA6