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- Bhatnagar, Amit, et al.
(författare)
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Removal of phenolic pollutants from water utilizing Mangifera indica (Mango) seed waste and cement fixation
- 2009
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Ingår i: Separation science and technology (Print). - : Informa UK Limited. - 0149-6395 .- 1520-5754. ; 44:13, s. 3150-3169
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Tidskriftsartikel (refereegranskat)abstract
- A process for the removal of two chlorophenols (2-chlorophenol and 2,4-dichlorophenol) from water using surface modified mango seed waste by adsorption process followed by cement fixation of the phenols-laden adsorbent is investigated. The two main objectives of this study were to develop efficient adsorbent utilizing mango seed waste by physiochemical activation and to an environmentally-friendly disposal of phenols-laden adsorbent into cement by a fixation process. The results of the present study reveal that the modified mango seed adsorbent showed an efficient adsorption potential for chlorophenols removal from water. The maximum adsorption potential of modified mango seed adsorbent for 2-chlorophenol and 2,4-dichlorophenol was 40.6 and 72.3 mg g−1, respectively at 25°C. Adsorption kinetic data of chlorophenols adsorption on mango seed adsorbent could be described more favorably by a pseudo-second-order kinetic model. After the adsorption studies, the phenol-laden adsorbent was immobilized in cement for its ultimate disposal. Leachates from the fixed phenols-laden adsorbent exhibit phenols concentrations lower than the drinking water standards. Results from this study suggest the potential utility of agricultural wastes as one of the most promising activated carbon precursors for phenols removal from water and wastewater and the safe disposal of phenol-laden adsorbent into cement by fixation process.
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- Campbell, PJ, et al.
(författare)
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Pan-cancer analysis of whole genomes
- 2020
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Ingår i: Nature. - : Springer Science and Business Media LLC. - 1476-4687 .- 0028-0836. ; 578:7793, s. 82-
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Tidskriftsartikel (refereegranskat)abstract
- Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale1–3. Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4–5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter4; identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation5,6; analyses timings and patterns of tumour evolution7; describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity8,9; and evaluates a range of more-specialized features of cancer genomes8,10–18.
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