Zobrazeno 1 - 10
of 2 547
pro vyhledávání: '"Surkov AN"'
Autor:
Surkov, Viacheslav, Wendler, Chris, Terekhov, Mikhail, Deschenaux, Justin, West, Robert, Gulcehre, Caglar
Sparse autoencoders (SAEs) have become a core ingredient in the reverse engineering of large-language models (LLMs). For LLMs, they have been shown to decompose intermediate representations that often are not interpretable directly into sparse sums o
Externí odkaz:
http://arxiv.org/abs/2410.22366
Autor:
Surkov, Egor
We provide a lower bound for the first eigenvalue of the Laplace-Beltrami operator on a closed orientable hypersurface minimally embedded in an orientable compact Riemannian manifold with Ricci curvature bounded below by a positive constant.
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Com
Externí odkaz:
http://arxiv.org/abs/2409.16419
Autor:
Davidson, Tim R., Surkov, Viacheslav, Veselovsky, Veniamin, Russo, Giuseppe, West, Robert, Gulcehre, Caglar
A rapidly growing number of applications rely on a small set of closed-source language models (LMs). This dependency might introduce novel security risks if LMs develop self-recognition capabilities. Inspired by human identity verification methods, w
Externí odkaz:
http://arxiv.org/abs/2407.06946
Autor:
Semenkin, Anton, Bibaev, Vitaliy, Sokolov, Yaroslav, Krylov, Kirill, Kalina, Alexey, Khannanova, Anna, Savenkov, Danila, Rovdo, Darya, Davidenko, Igor, Karnaukhov, Kirill, Vakhrushev, Maxim, Kostyukov, Mikhail, Podvitskii, Mikhail, Surkov, Petr, Golubev, Yaroslav, Povarov, Nikita, Bryksin, Timofey
In recent years, several industrial solutions for the problem of multi-token code completion appeared, each making a great advance in the area but mostly focusing on cloud-based runtime and avoiding working on the end user's device. In this work, we
Externí odkaz:
http://arxiv.org/abs/2405.08704
Autor:
Surkov, Maxim K., Yamshchikov, Ivan P.
Evaluation plays a significant role in modern natural language processing. Most modern NLP benchmarks consist of arbitrary sets of tasks that neither guarantee any generalization potential for the model once applied outside the test set nor try to mi
Externí odkaz:
http://arxiv.org/abs/2402.14890
Autor:
Maxim K. Surkov
Publikováno v:
Naučno-tehničeskij Vestnik Informacionnyh Tehnologij, Mehaniki i Optiki, Vol 24, Iss 5, Pp 758-769 (2024)
The task of automatic metainformation recognition from audio sources is to detect and extract data of various natures (speech, noises, acoustic scenes, acoustic events, anomalies) from a given audio input signal. This area is well developed and kno
Externí odkaz:
https://doaj.org/article/bf33ba510ce8430dbea5a9ae18304a00
Autor:
Nataliya V. Zhurkova, Nato V. Vashakmadze, Andrey N. Surkov, Tatiana V. Turti, Kristina V. Bogdanova, Yuliya Yu. Kotalevskaya, Ekaterina Yu. Zakharova, Leyla S. Namazova-Baranova
Publikováno v:
Вопросы современной педиатрии, Vol 23, Iss 3, Pp 188-196 (2024)
Background. Niemann-Pick disease, type A is a rare hereditary disease from the group of lysosomal storage diseases, it is characterized by early onset and progressive course. Description of this disease’s clinical cases is crucial for early diagnos
Externí odkaz:
https://doaj.org/article/6f938547a3b7411995ac4e87c59b3a44
Autor:
Anatoly I. Khavkin, Anastasiya A. Permyakova, Mariya O. Tsepilova, Aleksandra V. Kaplina, Stanislav I. Sitkin, Andrey N. Surkov, Stanislav D. Getmanov
Publikováno v:
Вопросы современной педиатрии, Vol 23, Iss 3, Pp 145-151 (2024)
Nowadays, an urgent problem of pediatric gastroenterology is the study of inflammatory bowel diseases with very early onset (VEO-IBD), which have unique genetic, clinical, immunological, morphological, and laboratory sings. Early VEO-IBD is usually c
Externí odkaz:
https://doaj.org/article/842641a971ca452f885777c08f4d0908
Autor:
Andrey N. Surkov, Leyla S. Namazova-Baranova, Anna L. Arakelyan, Evgeny E. Bessonov, Natalia V. Zhurkova
Publikováno v:
Вопросы современной педиатрии, Vol 23, Iss 3, Pp 162-167 (2024)
Glycogen storage disease type Ib (GSD Ib) is a rare and extremely severe disease included in the group of hereditary carbohydrate metabolism disorders. The condition is caused by pathogenic variants in the SLC37A4 gene leading to glucose metabolic di
Externí odkaz:
https://doaj.org/article/8b4ab6f90c7b4f8b855be3182c18ab2f
Autor:
Natalia A. Averkina, Madlena E. Bagaeva, Aleksander A. Baranov, Nato D. Vashakmadze, Elena A. Vishneva, Olga S. Gundobina, Nataliya V. Zhurkova, Elena V. Kaitukova, Elena V. Komarova, Tea V. Margieva, Leyla S. Namazova-Baranova, Valeria P. Novikova, Elena E. Petryaykina, Mariya M. Platonova, Aleksander S. Potapov, Olga Ya. Smirnova, Tatiana V. Strokova, Andrey N. Surkov, Nataliya N. Taran, Marina V. Fedoseenko, Nataliya A. Semenova, Inga V. Anisimova, Svetlana A. Repina, Dmitriy M. Subbotin, Valeria V. Sviridova, Anatoliy I. Havkin, Ekaterina A. Yablokova, Galina V. Volynets, Irina V. Sadovnikova, Elena L. Tumanova
Publikováno v:
Педиатрическая фармакология, Vol 21, Iss 3, Pp 263-288 (2024)
Glycogen storage disease refers to hereditary pathologies of carbohydrate metabolism, its cause is mutations of various genes encoding enzymes responsible for the synthesis and breakdown of glycogen. Due to enzyme defects, excessive glycogen depositi
Externí odkaz:
https://doaj.org/article/2285f6ae182245fcb31dc23d242e513c