Advantages |
Species- or transcript-specific probes are not required in the case of NGS technology. |
Specific probes are required in the case of microarray technologies. |
NGS technology computes the sequencing read counts, analyzing the result for studying gene expression. |
Gene expression measurement based on array hybridization technology is restricted by background and signal saturation noise. |
NGS shows increased specificity and sensitivity for wide range of applications. |
Specificity and sensitivity is low as compared to NGS for identifying differentially expressed genes. |
Sequencing coverage depth is high in NGS technology facilitating the detection of rare or single transcripts per cell as well as in identifying weakly expressed genes. |
Rare and low-abundance transcripts cannot be easily detected and are lost using microarray technology. |
NGS technology is able to detect multiple splice sites and novel isoforms. |
Microarray technologies cannot detect multiple splice sites and novel isoforms. |
NGS technology is able to do de novo analysis of sample without reference genome. |
Reference genome is required for the analysis of sample. |
Disadvantages |
NGS based techniques are very expensive. |
Microarrays are cheaper in comparison to NGS. |
Accuracy and longevity of this approach remains questionable. |
Microarray is more reliable methods in long run. |
Low yield of high-quality sequences are obtained using NGS techniques. |
Comparatively high yield of high-quality sequences is obtained using microarray technologies. |
NGS technologies have a drawback of generating shorter sequences with more noise. |
Microarray offers lesser errors and is more accurate. |
NGS assembly algorithms show poor performance in presence of identical repeats. |
Homologous repeats are identified using microarray technologies. |
Annotation is challenging when considering complex genomes with higher repeat and duplication content. |
Microarray technologies are more successful when considering complex genomes with higher repeat and duplication content. |