Difference between revisions of "Team:NCTU Formosa/Dry Lab/NGS Data Analysis"

     To train our model more effectively, we use NGS 16s to analyze the microbiota in the soil. We spray biostimulators into the soil to affect the entire microbiota and use NGS 16s regularly. By analyzing multiple NGS data, we can determine the nature of the relationships about bacteria and take advantage of these characteristics to add biostimulators again. Through this process training our model, we adjust to our system again and again, allowing our system predicts the changes of microbiota in soil accurately.

     Next, we will interpret NGS and 16S rRNA separately.

NGS
   NGS(Next Generation Sequencing) is a kind of technique to sequence a number of genomes in very short time. There are three main platforms on the market currently: Solexa from Illumina, SOLiD from ABI, and 454 from Roche. The procedures of these three sequencers are different, but they are all based on chain termination. Take Solixa for example, following these steps below:

1. Use ultrasound to break original DNA sequences into fragments of about 200-500 base pairs, and then attach the adapters to both ends of the fragments.

2. Place the DNA fragments on a flowcell with complementary adapter sequences on the surface. The adapters will adhere to each other to allow the DNA fragments stay at the flow cell.

3. Amplify DNA fragments by bridge amplification.

4. The sequencing uses the method like the Sanger sequencing, adding different bases (dNTPs) and synthetic reagents that have been calibrated for specific removable fluorescent molecules. Repeatedly the process of removing and detecting fluorescence. Last, the computer software will analysis large numbers of DNA sequences quickly.

FASTQC
     FASTQC is mainly used to filter the NGS data. It is very important to check the data quality before analyzing the data. If the data quality is high , you can continue the next step.
    After we input NGS sequence data into FASTQC, the program will analyze automatically and score each sequence to ensure that the quality of the gene sequences is suitable for computer calculation.

16S rRNA
   16S rRNA is an important component of the ribosomal small subunit of prokaryote. The sequence contains several conserved regions and 9 hypervariable regions (V1 to V9). The hypervariable regions have genus or species specificity, considered to be the most suitable indicator for phylogeny of bacteria and identification of classification. NGS 16s uses the sequence of V4 and V5 in the hypervariable regions to detect the bacterial clusters.

Sampling
     We divide the agricultural land into four large blocks of A, B, C, and D. In each block, there are three strips of 1, 2, and 3, each of which is divided into T, M, and D. Thus, we have thirty six sample in total( A1T, A2M, ....). We get 50 micro liters per sample from 10 to 15 centimeters depth near the root of each testing plant. Then, the samples are sent to the company for NGS analysis.

     The result will present the each bacteria ratio in each samples and report it in an OTU table.(Fig. 1)

     Microbiome data are generated from 16S ribosomal RNA(rRNA) gene. The PCR primers were designed to amplify the V4 region of the bacterial 16S ribosomal DNA. After profiling 16S rRNA sequencing, we used QIIME to generate operational taxonomic units (OTUs) table. Then we used bioinformatics tools and statistics methods to analyze microbial diversity in soil samples. We also used machine learning to predict how soil microbiota changes with addition of bio-stimulators.

     Figure 1 is an example of OTUs table. Each column represents the type and amount of bacteria (OTU1, OTU2, …, OTU7) in each soil sample (A1, A2, A3, B1, B2, and B3). We generate seven tables for each level: Phylum, Class, Order, Family, Genus, and Species.

     The OTUs tables will consist of unclassified names using the open source pipeline of QIIME. Thus, we have to rearrange the data to facilitate analysis according to the following steps:
     Step 1. Delete unclassified genomic segments.
     Step 2. Calculate the ratios of the remaining entries.
     Step 3. Select the most abundant bacteria within soil samples to observe
     their distribution using the following bar charts (Fig. 3). After making the Stacked bar, we organized the data to facilitate the analysis (Table 1). We observed growths and declines of bacteria in the soil, and then summarized the bacteria according to their functions. Moreover, we will explain what we do in our farm affect microbiota. For example: Sphingomonas, Alcanivorax, Devosia which are polluting indicator bacteria, are decreased continuously from May to July. We speculate that the reason of their decline is that we have not applied herbicides, pesticides or other pollutants in these three months. When the soil repaired by itself, the pollutants are falling, and the polluting indicator bacteria are also falling. After the series of analysis, we hope to prove the basic hypothesis of our project--we can precisely regulate microbiota in the soil by using bio-stimulator. We will put our details of analysis in our demonstration.

     The strength of co-occurrence of bacteria within soil samples was evaluated by the Spearman’s rank correlation coefficients. It ranges from -1 to 1. The formula of Spearman correlation coefficient is as follows:

     Then we use heat maps to visualize the correlation strengths. Figure 4 shows the 20 most abundant bacteria within soil samples.
     A computer program can then visualize the results in a heat map. A map of the 20 most abundant bacteria of our soil is shown below: