1,248 skills found · Page 1 of 42
vllm-project / VllmA high-throughput and memory-efficient inference and serving engine for LLMs
microsoft / GarnetGarnet is a remote cache-store from Microsoft Research that offers strong performance (throughput and latency), scalability, storage, recovery, cluster sharding, key migration, and replication features. Garnet can work with existing Redis clients.
FMInference / FlexLLMGenRunning large language models on a single GPU for throughput-oriented scenarios.
MystenLabs / SuiSui, a next-generation smart contract platform with high throughput, low latency, and an asset-oriented programming model powered by the Move programming language
rsalmei / Alive ProgressA new kind of Progress Bar, with real-time throughput, ETA, and very cool animations!
awslabs / Mountpoint S3A simple, high-throughput file client for mounting an Amazon S3 bucket as a local file system.
readysettech / ReadysetReadyset is a MySQL and Postgres wire-compatible caching layer that sits in front of existing databases to speed up queries and horizontally scale read throughput. Under the hood, ReadySet caches the results of cached select statements and incrementally updates these results over time as the underlying data changes.
rosedblabs / RosedbLightweight, fast and reliable key/value storage engine based on Bitcask.
giltene / Wrk2A constant throughput, correct latency recording variant of wrk
eclipse-openj9 / Openj9Eclipse OpenJ9: A Java Virtual Machine for OpenJDK that's optimized for small footprint, fast start-up, and high throughput. Builds on Eclipse OMR (https://github.com/eclipse/omr) and combines with the Extensions for OpenJDK for OpenJ9 repo.
NAalytics / Assemblies Of Putative SARS CoV2 Spike Encoding MRNA Sequences For Vaccines BNT 162b2 And MRNA 1273RNA vaccines have become a key tool in moving forward through the challenges raised both in the current pandemic and in numerous other public health and medical challenges. With the rollout of vaccines for COVID-19, these synthetic mRNAs have become broadly distributed RNA species in numerous human populations. Despite their ubiquity, sequences are not always available for such RNAs. Standard methods facilitate such sequencing. In this note, we provide experimental sequence information for the RNA components of the initial Moderna (https://pubmed.ncbi.nlm.nih.gov/32756549/) and Pfizer/BioNTech (https://pubmed.ncbi.nlm.nih.gov/33301246/) COVID-19 vaccines, allowing a working assembly of the former and a confirmation of previously reported sequence information for the latter RNA. Sharing of sequence information for broadly used therapeutics has the benefit of allowing any researchers or clinicians using sequencing approaches to rapidly identify such sequences as therapeutic-derived rather than host or infectious in origin. For this work, RNAs were obtained as discards from the small portions of vaccine doses that remained in vials after immunization; such portions would have been required to be otherwise discarded and were analyzed under FDA authorization for research use. To obtain the small amounts of RNA needed for characterization, vaccine remnants were phenol-chloroform extracted using TRIzol Reagent (Invitrogen), with intactness assessed by Agilent 2100 Bioanalyzer before and after extraction. Although our analysis mainly focused on RNAs obtained as soon as possible following discard, we also analyzed samples which had been refrigerated (~4 ℃) for up to 42 days with and without the addition of EDTA. Interestingly a substantial fraction of the RNA remained intact in these preparations. We note that the formulation of the vaccines includes numerous key chemical components which are quite possibly unstable under these conditions-- so these data certainly do not suggest that the vaccine as a biological agent is stable. But it is of interest that chemical stability of RNA itself is not sufficient to preclude eventual development of vaccines with a much less involved cold-chain storage and transportation. For further analysis, the initial RNAs were fragmented by heating to 94℃, primed with a random hexamer-tailed adaptor, amplified through a template-switch protocol (Takara SMARTerer Stranded RNA-seq kit), and sequenced using a MiSeq instrument (Illumina) with paired end 78-per end sequencing. As a reference material in specific assays, we included RNA of known concentration and sequence (from bacteriophage MS2). From these data, we obtained partial information on strandedness and a set of segments that could be used for assembly. This was particularly useful for the Moderna vaccine, for which the original vaccine RNA sequence was not available at the time our study was carried out. Contigs encoding full-length spikes were assembled from the Moderna and Pfizer datasets. The Pfizer/BioNTech data [Figure 1] verified the reported sequence for that vaccine (https://berthub.eu/articles/posts/reverse-engineering-source-code-of-the-biontech-pfizer-vaccine/), while the Moderna sequence [Figure 2] could not be checked against a published reference. RNA preparations lacking dsRNA are desirable in generating vaccine formulations as these will minimize an otherwise dramatic biological (and nonspecific) response that vertebrates have to double stranded character in RNA (https://www.nature.com/articles/nrd.2017.243). In the sequence data that we analyzed, we found that the vast majority of reads were from the expected sense strand. In addition, the minority of antisense reads appeared different from sense reads in lacking the characteristic extensions expected from the template switching protocol. Examining only the reads with an evident template switch (as an indicator for strand-of-origin), we observed that both vaccines overwhelmingly yielded sense reads (>99.99%). Independent sequencing assays and other experimental measurements are ongoing and will be needed to determine whether this template-switched sense read fraction in the SmarterSeq protocol indeed represents the actual dsRNA content in the original material. This work provides an initial assessment of two RNAs that are now a part of the human ecosystem and that are likely to appear in numerous other high throughput RNA-seq studies in which a fraction of the individuals may have previously been vaccinated. ProtoAcknowledgements: Thanks to our colleagues for help and suggestions (Nimit Jain, Emily Greenwald, Lamia Wahba, William Wang, Amisha Kumar, Sameer Sundrani, David Lipman, Bijoyita Roy). Figure 1: Spike-encoding contig assembled from BioNTech/Pfizer BNT-162b2 vaccine. Although the full coding region is included, the nature of the methodology used for sequencing and assembly is such that the assembled contig could lack some sequence from the ends of the RNA. Within the assembled sequence, this hypothetical sequence shows a perfect match to the corresponding sequence from documents available online derived from manufacturer communications with the World Health Organization [as reported by https://berthub.eu/articles/posts/reverse-engineering-source-code-of-the-biontech-pfizer-vaccine/]. The 5’ end for the assembly matches the start site noted in these documents, while the read-based assembly lacks an interrupted polyA tail (A30(GCATATGACT)A70) that is expected to be present in the mRNA.
michaelfeil / InfinityInfinity is a high-throughput, low-latency serving engine for text-embeddings, reranking models, clip, clap and colpali
deepspeedai / DeepSpeed MIIMII makes low-latency and high-throughput inference possible, powered by DeepSpeed.
Tencent / PhxqueueA high-availability, high-throughput and highly reliable distributed queue based on the Paxos algorithm.
didi / DDMQDDMQ is a distributed messaging product with low latency, high throughput and high availability.
bregman-arie / System Design NotebookLearn System Design step by step
Soul-AILab / SoulX FlashTalkSoulX-FlashTalk is the first 14B model to achieve sub-second start-up latency (0.87s) while maintaining a real-time throughput of 32 FPS on an 8xH800 node.
Zilliqa / Zq1Zilliqa is the world's first high-throughput public blockchain platform - designed to scale to thousands of transactions per second.
rari-build / Rarirari: High-performance React Server Components framework powered by a Rust runtime, delivering 8.7x faster response times (0.14ms vs 1.22ms) and 44.9x higher throughput (67,208 vs 1,496 req/sec) than Next.js with zero-config setup.
broadinstitute / PicardA set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
