New insights into electron spin dynamics in the presence of correlated noise

The changes of the spin depolarization length in zinc-blende semiconductors when an external component of correlated noise is added to a static driving electric field are analyzed for different values of field strength, noise amplitude and correlation time. Electron dynamics is simulated by a Monte Carlo procedure which keeps into account all the possible scattering phenomena of the hot electrons in the medium and includes the evolution of spin polarization. Spin depolarization is studied by examinating the decay of the initial spin polarization of the conduction electrons through the D'yakonov-Perel process, the only relevant relaxation mechanism in III-V crystals. Our results show that, for electric field amplitude lower than the Gunn field, the dephasing length shortens with the increasing of the noise intensity. Moreover, a nonmonotonic behavior of spin depolarization length with the noise correlation time is found, characterized by a maximum variation for values of noise correlation time comparable with the dephasing time. Instead, in high field conditions, we find that, critically depending on the noise correlation time, external fluctuations can positively affect the relaxation length. The influence of the inclusion of the electron-electron scattering mechanism is also shown and discussed.Comment: Published on "Journal of Physics: Condensed Matter" as "Fast Track Communications", 11 pages, 9 figure

Effect of phyto additives and Saccharomyces cerevisiae on rumen ferementation and microbial profile in buffaloes

To study the effect of plants containing plant secondary metabolites (PSM) and Saccharomyces cerevisiae on rumen ferementation and microbial profile, four fistulated adult buffaloes were fed in 4×4 Latin square design. The four groups were, control, without additive; T1, mixture of harad seed pulp and garlic bulb (2% of DMI); T2, S. cerevisiae (350g feremented feed containing S. cerevisiae 106 /g); T3, mixture of harad seed pulp, garlic bulb and S. cerevisiae. All the animals were fed on a basal diet consisting of wheat straw and concentrate mixture in 50:50 ratio. Daily DM intake was similar in all the four groups. Feeding of any of the dietary treatments did not affect rumen fluid pH, concentration of ammonia N and lactic acid. The total volatile fatty acids and its fractions except butyrate were also not influenced by supplementation of any of the additives. The activities of ruminal enzymes viz. carboxymethylcellulase, xylanase, avicelase and acetyl esterase were similar in all the four groups. The rumen microbial density of total bacteria, Ruminococcus flavefaciences, R. albus, methanogens and fungi were not changed whereas Fibrobacter succinogenes and protozoa populations were significantly reduced in T1 but were at par of control by inclusion of yeast in the diet. It is concluded that mixture of harad and garlic alone or in combination with yeast culture did not influence rumen fermentation however microbial profile (F. succinogenes and protozoa) was improved by feeding yeast as additive. The additives tested seem to have potential to alter rumen microbial ecology and can further be explored for its efficacy in improving the performance of the animals

Third-generation RNA-sequencing analysis : graph alignment and transcript assembly with long reads

The information contained in the genome of an organism, its DNA, is expressed through transcription of its genes to RNA, in quantities determined by many internal and external factors. As such, studying the gene expression can give valuable information for e.g. clinical diagnostics. A common analysis workflow of RNA-sequencing (RNA-seq) data consists of mapping the sequencing reads to a reference genome, followed by the transcript assembly and quantification based on these alignments. The advent of second-generation sequencing revolutionized the field by reducing the sequencing costs by 50,000-fold. Now another revolution is imminent with the third-generation sequencing platforms producing an order of magnitude higher read lengths. However, higher error rate, higher cost and lower throughput compared to the second-generation sequencing bring their own challenges. To compensate for the low throughput and high cost, hybrid approaches using both short second-generation and long third-generation reads have gathered recent interest. The first part of this thesis focuses on the analysis of short-read RNA-seq data. As short-read mapping is an already well-researched field, we focus on giving a literature review of the topic. For transcript assembly we propose a novel (at the time of the publication) approach of using minimum-cost flows to solve the problem of covering a graph created from the read alignments with a set of paths with the minimum cost, under some cost model. Various network-flow-based solutions were proposed in parallel to, as well as after, ours. The second part, where the main contributions of this thesis lie, focuses on the analysis of long-read RNA-seq data. The driving point of our research has been the Minimum Path Cover with Subpath Constraints (MPC-SC) model, where transcript assembly is modeled as a minimum path cover problem, with the addition that each of the chains of exons (subpath constraints) created from the long reads must be completely contained in a solution path. In addition to implementing this concept, we experimentally studied different approaches on how to find the exon chains in practice. The evaluated approaches included aligning the long reads to a graph created from short read alignments instead of the reference genome, which led to our final contribution: extending a co-linear chaining algorithm from between two sequences to between a sequence and a directed acyclic graph.Transkriptiossa organismin geenien mallin mukaan luodaan RNA-molekyyleja. Lukuisat tekijät, sekä solun sisäiset että ulkoiset, määrittävät mitä geenejä transkriptoidaan, ja missä määrin. Tämän prosessin tutkiminen antaa arvokasta tietoa esimerkiksi lääketieteelliseen diagnostiikkaan. Yksi yleisistä RNA-sekvensointidatan analyysitavoista koostuu kolmesta osasta: lukujaksojen (read sequences) linjaus referenssigenomiin, transkriptien kokoaminen, ja transkriptien ekspressiotasojen määrittäminen. Toisen sukupolven sekvensointiteknologian kehityksen myötä sekvensoinnin hinta laski huomattavasti, mikä salli RNA-sekvensointidatan käytön yhä useampaan tarkoitukseen. Nyt kolmannen sukupolven sekvensointiteknologiat tarjoavat kertaluokkaa pidempiä lukujaksoja, mikä laajentaa analysointimahdollisuuksia. Kuitenkin suurempi virhemäärä, korkeampi hinta ja pienempi määrä tuotettua dataa tuovat omat haasteensa. Toisen ja kolmannen sukupolven teknologioiden käyttäminen yhdessä, ns. hybridilähestymistapa, on tutkimussuunta joka on kerännyt paljon kiinnostusta viimeaikoina. Tämän tutkielman ensimmäinen osa keskittyy toisen sukupolven, eli ns. lyhyiden RNA-lukujaksojen (short read), analyysiin. Näiden lyhyiden lukujaksojen linjausta referenssigenomiin on tutkittu jo 2000-luvulla, joten tällä alueella keskitymme olemassaolevaan kirjallisuuteen. Transkriptien kokoamisen alalta esittelemme metodin, joka käyttää vähimmäiskustannusvirtauksen (minimum-cost flow) mallia. Vähimmäiskustannusvirtauksen mallissa lukujaksoista luotu verkko peitetään joukolla polkuja, joiden kustannus on pienin mahdollinen. Virtausmalleja on käytetty myös muiden tutkijoiden kehittämissä analyysityökaluissa. Tämän tutkielman suurin kontribuutio on toisessa osassa, joka keskittyy ns. pitkien RNA-lukujaksojen (long read) analysointiin. Tutkimuksemme lähtökohtana on ollut malli, jossa pienimmän polkupeitteen (Minimum Path Cover) ongelmaan lisätään alipolkurajoitus (subpath constraint). Jokainen alipolkurajoitus vastaa eksoniketjua (exon chain), jotka jokin pitkä lukujakso peittää, ja jokaisen alipolkurajoituksen täytyy sisältyä kokonaan johonkin polkupeitteen polkuun. Tämän konseptin toteuttamisen lisäksi testasimme kokeellisesti erilaisia lähestymistapoja eksoniketjujen löytämiseksi. Näihin testattaviin lähestymistapoihin kuului pitkien lukujaksojen linjaaminen suoraan lyhyistä lukujaksoista luotuun verkkoon referenssigenomin sijaan. Tämä lähestymistapa johti tämän tutkielman viimeiseen kontribuutioon: kolineaarisen ketjun (co-linear chaining) algoritmin yleistäminen kahden sekvenssin sijasta sekvenssiin ja suunnattuun syklittömään verkkoon

Inducible expression of Pisum sativum xyloglucan fucosyltransferase in the pea root cap meristem, and effects of antisense mRNA expression on root cap cell wall structural integrity

Mitosis and cell wall synthesis in the legume root cap meristem can be induced and synchronized by the nondestructive removal of border cells from the cap periphery. Newly synthesized cells can be examined microscopically as they differentiate progressively during cap development, and ultimately detach as a new population of border cells. This system was used to demonstrate that Pisum sativum L. fucosyl transferase (PsFut1) mRNA expression is strongly expressed in root meristematic tissues, and is induced >2-fold during a 5-h period when mitosis in the root cap meristem is increased. Expression of PsFut1 antisense mRNA in pea hairy roots under the control of the CaMV35S promoter, which exhibits meristem localized expression in pea root caps, resulted in a 50–60% reduction in meristem localized endogenous PsFut1 mRNA expression measured using whole mount in situ hybridization. Changes in gross levels of cell wall fucosylated xyloglucan were not detected, but altered surface localization patterns were detected using whole mount immunolocalization with CCRC-M1, an antibody that recognizes fucosylated xyloglucan. Emerging hairy roots expressing antisense PsFut1 mRNA appeared normal macroscopically but scanning electron microscopy of tissues with altered CCRC-M1 localization patterns revealed wrinkled, collapsed cell surfaces. As individual border cells separated from the cap periphery, cell death occurred in correlation with extrusion of cellular contents through breaks in the wall

Beyond the "Code": A Guide to the Description and Documentation of Biodiversity in Ciliated Protists (Alveolata, Ciliophora)

© 2017 The International Society of Protistologists.Recent advances in molecular technology have revolutionized research on all aspects of the biology of organisms, including ciliates, and created unprecedented opportunities for pursuing a more integrative approach to investigations of biodiversity. However, this goal is complicated by large gaps and inconsistencies that still exist in the foundation of basic information about biodiversity of ciliates. The present paper reviews issues relating to the taxonomy of ciliates and presents specific recommendations for best practice in the observation and documentation of their biodiversity. This effort stems from a workshop that explored ways to implement six Grand Challenges proposed by the International Research Coordination Network for Biodiversity of Ciliates (IRCN-BC). As part of its commitment to strengthening the knowledge base that supports research on biodiversity of ciliates, the IRCN-BC proposes to populate The Ciliate Guide, an online database, with biodiversity-related data and metadata to create a resource that will facilitate accurate taxonomic identifications and promote sharing of data

Effect of angiotensin-converting enzyme inhibitor and angiotensin receptor blocker initiation on organ support-free days in patients hospitalized with COVID-19

IMPORTANCE Overactivation of the renin-angiotensin system (RAS) may contribute to poor clinical outcomes in patients with COVID-19. Objective To determine whether angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) initiation improves outcomes in patients hospitalized for COVID-19. DESIGN, SETTING, AND PARTICIPANTS In an ongoing, adaptive platform randomized clinical trial, 721 critically ill and 58 non–critically ill hospitalized adults were randomized to receive an RAS inhibitor or control between March 16, 2021, and February 25, 2022, at 69 sites in 7 countries (final follow-up on June 1, 2022). INTERVENTIONS Patients were randomized to receive open-label initiation of an ACE inhibitor (n = 257), ARB (n = 248), ARB in combination with DMX-200 (a chemokine receptor-2 inhibitor; n = 10), or no RAS inhibitor (control; n = 264) for up to 10 days. MAIN OUTCOMES AND MEASURES The primary outcome was organ support–free days, a composite of hospital survival and days alive without cardiovascular or respiratory organ support through 21 days. The primary analysis was a bayesian cumulative logistic model. Odds ratios (ORs) greater than 1 represent improved outcomes. RESULTS On February 25, 2022, enrollment was discontinued due to safety concerns. Among 679 critically ill patients with available primary outcome data, the median age was 56 years and 239 participants (35.2%) were women. Median (IQR) organ support–free days among critically ill patients was 10 (–1 to 16) in the ACE inhibitor group (n = 231), 8 (–1 to 17) in the ARB group (n = 217), and 12 (0 to 17) in the control group (n = 231) (median adjusted odds ratios of 0.77 [95% bayesian credible interval, 0.58-1.06] for improvement for ACE inhibitor and 0.76 [95% credible interval, 0.56-1.05] for ARB compared with control). The posterior probabilities that ACE inhibitors and ARBs worsened organ support–free days compared with control were 94.9% and 95.4%, respectively. Hospital survival occurred in 166 of 231 critically ill participants (71.9%) in the ACE inhibitor group, 152 of 217 (70.0%) in the ARB group, and 182 of 231 (78.8%) in the control group (posterior probabilities that ACE inhibitor and ARB worsened hospital survival compared with control were 95.3% and 98.1%, respectively). CONCLUSIONS AND RELEVANCE In this trial, among critically ill adults with COVID-19, initiation of an ACE inhibitor or ARB did not improve, and likely worsened, clinical outcomes. TRIAL REGISTRATION ClinicalTrials.gov Identifier: NCT0273570