bastetfurry's Stars
sanni/cartreader
A shield for the Arduino Mega that can back up video game cartridges.
hoglet67/RGBtoHDMI
Bare-metal Raspberry Pi project that provides pixel-perfect sampling of Retro Computer RGB/YUV video and conversion to HDMI
captain-amygdala/pistorm
68k Hardware Emulator
lino/serious-agile-methods
this is a collection of serious agile methods which you can use to run your company into the ground like a professional consultant without having to pay an arm and a leg for it
sblendorio/gorilla-cpm
GORILLA.BAS port to CP/M in Turbo Modula-2. Supported terminals: VT52, VT100, ANSI, ADM-31, KayPro, C128, Memotech monochrome, CPC / Zenith Z19
NAalytics/Assemblies-of-putative-SARS-CoV2-spike-encoding-mRNA-sequences-for-vaccines-BNT-162b2-and-mRNA-1273
RNA 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.
DarkPacks/SevTech-Ages
SevTech: Ages is a massive Minecraft modpack packed with content and progression.
GClown25/BIT4
BIT4 is a 4Bit microcontroller - fully programmable with only three buttons.
fnuecke/oc2
RISC-V VMs in Minecraft.
mmoskal/uf2-stm32f
UF2 bootloader for STM32F4
artemisamsx/artemisa
Schematics, PCB designs and HDL simulations to build a 8-bits MSX computer
beokim/kc87fpga
clarkm/dupepad
dupePad - Qwerty Frogpad clone for Mac & PC
ThomasKaiser/sbc-bench
Simple benchmark for single board computers
jhhoward/Faux86
A portable, open-source 8086 PC emulator for bare metal Raspberry Pi
awesome-selfhosted/awesome-selfhosted
A list of Free Software network services and web applications which can be hosted on your own servers
necroware/silly-sound-bastard
Yet another Covox Speech Thing clone
foone/CosmiPasswordDecoder
Decodes passwords for Cosmi multi-CDs
GDATASoftwareAG/MSE
Malware sample exchange system and API intended for Anti-Virus companies and researchers.
fbergama/pigfx
PiGFX is a bare metal kernel for the Raspberry Pi that implements a basic ANSI terminal emulator with the additional support of some primitive graphics functions.
peachpiecompiler/peachpie
PeachPie - the PHP compiler and runtime for .NET and .NET Core
GDATASoftwareAG/motornet
Motor.NET is a microservice framework based on Microsoft.Extensions.Hosting
dbuchwald/6502
DB6502: 65C02 based computer inspired by BE6502
GTAmodding/re3
GTA III, Vice City
misterblack1/ps2-to-tandy1000-keyboard
PS2/AT Keyboard to Tandy 1000 Keyboard Adapter
balintkissdev/awesome-dos
Curated list of references for development of DOS applications.
wwarthen/RomWBW
System Software for Z80/Z180/Z280 Computers
littlefs-project/littlefs
A little fail-safe filesystem designed for microcontrollers
sblendorio/petscii-bbs
A Java framework for building highly customizable PETSCII-enabled BBS, accessible from Commodore 64/128
pellepl/stm32_spiffs
STM32 target playground for spiffs