Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.7554/eLife.63409 http://scihub22266oqcxt.onion/10.7554/eLife.63409 33620031!7901870!33620031     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Elife 2021 ; 10 (ä): ä Nephropedia Template TP {{tp|p=33620031|t=2021. COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locations and dates of interest |pdf=|usr=}}{{33620031}} gab.com Text COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locations and dates of interest JO: Elife http://www.kidney.de/pget.php?&tw=1&pmid=33620031 #FOAvip COVID-19 CG (covidcg.org) is an open resource for tracking SARS-CoV-2 single-nucleotide variations (SNVs), lineages, and clades using the virus genomes on the GISAID database while filtering by location, date, gene, and mutation of interest. COVID-19 CG provides significant time, labor, and cost-saving utility to projects on SARS-CoV-2 transmission, evolution, diagnostics, therapeutics, vaccines, and intervention tracking. Here, we describe case studies in which users can interrogate (1) SNVs in the SARS-CoV-2 spike receptor binding domain (RBD) across different geographical regions to inform the design and testing of therapeutics, (2) SNVs that may impact the sensitivity of commonly used diagnostic primers, and (3) the emergence of a dominant lineage harboring an S477N RBD mutation in Australia in 2020. To accelerate COVID-19 efforts, COVID-19 CG will be upgraded with new features for users to rapidly pinpoint mutations as the virus evolves throughout the pandemic and in response to therapeutic and public health interventions. Twit Text FOAVip COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locations and dates of interest ????Elife http://www.kidney.de/pget.php?&tw=1&pmid=33620031 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33620031 #FOAvip English Wikipedia <ref>{{Cite pmid|33620031}}</ref> COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locations and dates of interest #MMPMID33620031 Chen AT; Altschuler K; Zhan SH; Chan YA; Deverman BE Elife 2021[Feb]; 10 (ä): ä PMID33620031show ga COVID-19 CG (covidcg.org) is an open resource for tracking SARS-CoV-2 single-nucleotide variations (SNVs), lineages, and clades using the virus genomes on the GISAID database while filtering by location, date, gene, and mutation of interest. COVID-19 CG provides significant time, labor, and cost-saving utility to projects on SARS-CoV-2 transmission, evolution, diagnostics, therapeutics, vaccines, and intervention tracking. Here, we describe case studies in which users can interrogate (1) SNVs in the SARS-CoV-2 spike receptor binding domain (RBD) across different geographical regions to inform the design and testing of therapeutics, (2) SNVs that may impact the sensitivity of commonly used diagnostic primers, and (3) the emergence of a dominant lineage harboring an S477N RBD mutation in Australia in 2020. To accelerate COVID-19 efforts, COVID-19 CG will be upgraded with new features for users to rapidly pinpoint mutations as the virus evolves throughout the pandemic and in response to therapeutic and public health interventions. |*Mutation[MESH] |Amino Acid Sequence[MESH] |Binding Sites/genetics[MESH] |COVID-19/epidemiology/*prevention & control/virology[MESH] |Computational Biology/*methods[MESH] |Genome, Viral/*genetics[MESH] |Geography[MESH] |Global Health[MESH] |Humans[MESH] |Internet[MESH] |Pandemics[MESH] |Patient Identification Systems/methods[MESH] |Phylogeny[MESH] |SARS-CoV-2/classification/*genetics/physiology[MESH] |Sequence Homology, Amino Acid[MESH] |Software[MESH]COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locati(epmc).pdf DeepDyve Pubget Overpricing