Modified Aggressive Packet Combining Scheme with Repetition Code for Throughput Enhancement in High Error Rate Channel

Author(s):  
Mancharla Ravi ◽  
Yaka Bulo
1993 ◽  
Vol 41 (6) ◽  
pp. 852-863 ◽  
Author(s):  
Q. Wang ◽  
G. Li ◽  
V.K. Bhargava ◽  
L.J. Mason

2021 ◽  
Author(s):  
Dan Levy ◽  
Zihua Wang ◽  
Andrea Moffitt ◽  
Michael H. Wigler

Replication of tandem repeats of simple sequence motifs, also known as microsatellites, is error prone and variable lengths frequently occur during population expansions. Therefore, microsatellite length variations could serve as markers for cancer. However, accurate error-free quantitation of microsatellite lengths is difficult with current methods because of a high error rate during amplification and sequencing. We have solved this problem by using partial mutagenesis to disrupt enough of the repeat structure so that it can replicate faithfully, yet not so much that the flanking regions cannot be reliably identified. In this work we use bisulfite mutagenesis to convert a C to a U, later read as T. Compared to untreated templates, we achieve three orders of magnitude reduction in the error rate per round of replication. By requiring two independent first copies of an initial template, we reach error rates below one in a million. We discuss potential clinical applications of this method.


1984 ◽  
Vol 20 (23) ◽  
pp. 986 ◽  
Author(s):  
M. Moeneclaey ◽  
H. Bruneel
Keyword(s):  

1981 ◽  
Vol 38 (9) ◽  
pp. 1168-1170 ◽  
Author(s):  
Harold E. Welch ◽  
Kenneth H. Mills

Fish can be permanently marked by scarring soft fin rays. Advantages over existing marking methods include rapidity of application, permanence, individual identification, low costs, and lack of adverse effects caused by the mark. Disadvantages include lack of recognition by untrained observers and a relatively high error rate when reading marks.Key words: fish marking, fin rays


1997 ◽  
Vol 8 (1) ◽  
pp. 3-7 ◽  
Author(s):  
John E. Hunter

The significance test as currently used is a disaster Whereas most researchers falsely believe that the significance test has an error rate of 5%, empirical studies show the average error rate across psychology is 60%–12 times higher than researchers think it to be The error rate for inference using the significance test is greater than the error rate using a coin toss to replace the empirical study The significance test has devastated the research review process Comprehensive reviews cite conflicting results on almost every issue Yet quantitatively accurate review of the same results shows that the apparent conflicts stem almost entirely from the high error rate for the significance test If 60% of studies falsely interpret their primary results, then reviewers who base their reviews on the interpreted study “findings” will have a 100% error rate in concluding that there is conflict between study results


2019 ◽  
Vol 85 (21) ◽  
Author(s):  
Kaire Loit ◽  
Kalev Adamson ◽  
Mohammad Bahram ◽  
Rasmus Puusepp ◽  
Sten Anslan ◽  
...  

ABSTRACT Culture-based molecular identification methods have revolutionized detection of pathogens, yet these methods are slow and may yield inconclusive results from environmental materials. The second-generation sequencing tools have much-improved precision and sensitivity of detection, but these analyses are costly and may take several days to months. Of the third-generation sequencing techniques, the portable MinION device (Oxford Nanopore Technologies) has received much attention because of its small size and possibility of rapid analysis at reasonable cost. Here, we compare the relative performances of two third-generation sequencing instruments, MinION and Sequel (Pacific Biosciences), in identification and diagnostics of fungal and oomycete pathogens from conifer (Pinaceae) needles and potato (Solanum tuberosum) leaves and tubers. We demonstrate that the Sequel instrument is efficient for metabarcoding of complex samples, whereas MinION is not suited for this purpose due to a high error rate and multiple biases. However, we find that MinION can be utilized for rapid and accurate identification of dominant pathogenic organisms and other associated organisms from plant tissues following both amplicon-based and PCR-free metagenomics approaches. Using the metagenomics approach with shortened DNA extraction and incubation times, we performed the entire MinION workflow, from sample preparation through DNA extraction, sequencing, bioinformatics, and interpretation, in 2.5 h. We advocate the use of MinION for rapid diagnostics of pathogens and potentially other organisms, but care needs to be taken to control or account for multiple potential technical biases. IMPORTANCE Microbial pathogens cause enormous losses to agriculture and forestry, but current combined culturing- and molecular identification-based detection methods are too slow for rapid identification and application of countermeasures. Here, we develop new and rapid protocols for Oxford Nanopore MinION-based third-generation diagnostics of plant pathogens that greatly improve the speed of diagnostics. However, due to high error rate and technical biases in MinION, the Pacific BioSciences Sequel platform is more useful for in-depth amplicon-based biodiversity monitoring (metabarcoding) from complex environmental samples.


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